Category: 626-01-7

Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons-Smith reaction (cyclopropanation using iodomethane), 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline. Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction. Safety of 3-Iodoaniline.

Zhang, Juan;Li, Xianfeng;Wei, Haimei;Li, Yangfeng;Zhang, Gong;Li, Yizhou research published 《 Sequential DNA-Encoded Building Block Fusion for the Construction of Polysubstituted Pyrazoline Core Libraries》, the research content is summarized as follows. Herein, a sequential DNA-encoded synthesis strategy for polysubstituted pyrazoline heterocycles, which fuses a broad panel of aldehydes, aryl amines, and alkenes as building blocks was reported. Furthermore, mock library synthesis and selection demonstrated the ability of the method to produce DNA-encoded focused libraries with highly functionalized pyrazoline cores.

Safety of 3-Iodoaniline, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline.Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles. Application In Synthesis of 626-01-7.

Zhang, Jun;Li, Yue;Wang, Bei;Jia, Ai-Quan;Zhang, Qian-Feng research published 《 Synthesis of Dichlorobenzamide Derivatives: Crystal Structures of 3,5-Dichloro-N-(2-chlorophenyl)benzamide and 3,5-Dichloro-N-(4-chlorophenyl)benzamide》, the research content is summarized as follows. Reactions of 3,5-dichlorobenzoyl chloride and arylamines in N,N’-dimethylformamide solution at 60°C afforded a series of dichlorobenzamide derivatives 3,5-di-ClC₆H₃C(O)NHR¹ [R¹ = Bn, 2,6-di-MeC₆H₃, 4-ClC₆H₄, etc.] in good yields. The dichlorobenzamides 3,5-di-ClC₆H₃C(O)NHR¹ [R¹ = 2-ClC₆H₄, 4-ClC₆H₄] were characterized by X-ray crystallog. The compound 3,5-di-ClC₆H₃C(O)NHR¹ [R¹ = 4-ClC₆H₄] crystallizes in triclinic space group P̅, with a = 5.047 (18), b = 10.28 (4), c = 13.36 (5) Å, α = 107.59 (5)°, β = 93.55 (5)°, γ = 98.34 (5)°, and Z = 2. The unit cell of compound 3,5-di-ClC₆H₃C(O)NHR¹ [R¹ = 2-ClC₆H₄] had a monoclinic Pn symmetry with cell parameters a = 9.581 (3), b = 12.217 (4), c = 11.072 (3) Å, β = 92.584 (4)°, and Z = 4.

Application In Synthesis of 626-01-7, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline.Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles. Electric Literature of 626-01-7.

Zhang, Tao;Wang, Yanhong;Wang, Bin;Jin, Weiwei;Xia, Yu;Liu, Chenjiang;Zhang, Yonghong research published 《 Visible-Light-Induced Oxidation of Diazenyl-Protected Tetrahydroisoquinolines and Isoindolines for the Synthesis of Functionalized Lactams》, the research content is summarized as follows. A visible-light-induced oxidation of diazenyl-protected tetrahydroisoquinolines and isoindolines for the synthesis of structurally diverse lactams I [R = H, 4-Me, 4-Et, etc.; R¹ = H, 6-Br, 5-Br, 6,7-di-MeO; n = 1, 2] was developed. The reaction was carried out with Eosin Y-Na₂ as an organic photocatalyst and mol. oxygen as an oxidant, and the desired functionalized N-aryldiazenyl-lactams were obtained under mild and transition metal-free conditions. The utility of this method was showcased by the gram-scale synthesis and deprotection of the N-aryldiazenyl-lactam product.

Electric Literature of 626-01-7, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs. Product Details of C6H6IN.

Zhang, Xianwen;Li, Ping;Xu, Bin;Wang, Jingxia;Fan, Guangyin;Zhang, Xiaobin;Liu, Xiaoqiang;Zhang, Kaiming;Jiang, Weidong research published 《 In Situ Hydrogen Activation Inspiring Efficient One-Pot Hydrogenation of Halogenated Nitrobenzenes over Ni-Co-Based Composites》, the research content is summarized as follows. Selective hydrogenation of halogenated nitrobenzenes (XNBs) to halogenated amines (XANs) is of great importance for practical applications. Non-noble metal-based catalysts have shown prominent advantages in price and reserves accompanying low activity and selectivity toward the hydrogenation of halogenated nitrobenzenes (XNBs) even under harsh conditions. In this work, inexpensive Ni-Co-based composites (N_xCC) were prepared for in situ tandem hydrogenation of XNBs to XANs by using hydrogen released from ammonia borane (AB) hydrolysis under ambient pressure. The results show these N_xCC samples exhibited superior catalytic performance against Co₃O₄ or NiO samples. A selected N_0.2CC catalyst as the mainly screened one can quant. convert XNBs to XANs with unprecedented activity with 100% XAN conversion. This catalyst can completely convert m-chloronitrobenzene (m-CNB) to m-chloroaniline (m-CAN), suggesting N_0.2CC efficiently suppresses the further dichlorination of m-CAN. Recycling test shows the N_0.2CC possesses higher stability and recyclability. The N_0.2CC catalyst was found to be a dual catalyst that synergistically catalyzes both the AB dehydrogenation (about 1735 mL min^-1 g^-1 of hydrogen generation rate) and the subsequent hydrogenation (almost 100% conversion) of XNBs. Notably, it is the first time that the rapid in situ hydrogen activation (IHA) which facilely arouses the efficient hydrogenation of adsorbed substrate on the surface of catalyst has been elaborated. From a unique perspective, distinctive and simple control experiments were innovatively designed for testifying the advantage of tandem hydrogenation in contrast with traditional hydrogenation. This work presents an efficient and environmental strategy to selectively produce XANs from XNBs using high-performance non-noble metal composites.

626-01-7, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., Product Details of C6H6IN

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

In general, organic iodides are light-sensitive and turn yellow during storage, owing to the formation of iodine. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline.Organic iodides can be alkyl, alkenyl, or alkynyl, and all of them are very reactive toward with many kinds of nucleophiles. Product Details of C6H6IN.

Zhang, Xuejie;Zhou, Yebin;Li, Guowei;Zhang, Lei;Yin, Chunyu;Yang, Yuanyuan;Wang, Hongzheng;Feng, Feng;Wei, Linwei;Zhang, Qunfeng;Yang, Feng;Lin, Lili;Lu, Chunshan;Li, Xiaonian research published 《 A highly sulfur resistant and stable heterogeneous catalyst for liquid-phase hydrogenation》, the research content is summarized as follows. Developing sulfur resistant and stable hydrogenation catalysts with a high activity is of great economic and environmental interest for the production of value-added fine chems., as it allows the use of crude industrial level raw materials as reactant, prevents environmental unfriendly stoichiometric reduction and cuts down energy-intensive separation/purification procedures. Here the authors show the metallic Ni nanoparticle well-enclosed in multilayer N doped graphene shells for the catalytic hydrogenation of nitrobenzene derivatives The nickel core promoted multilayer N doped graphene shell not only maintains the hydrogenation ability but also create a differentiate surface electronic state preventing the poisoning of vulnerable metal by S impurities. The catalytic performance has met the product requirement of hydrogenation of industrial raw materials including 4.00 weight% inorganic/organic sulfur poisoning substances, excessive acid residue and concentrated salts.

Product Details of C6H6IN, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Iodide is one of the largest monatomic anions. It is assigned a radius of around 206 picometers. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline.For comparison, the lighter halides are considerably smaller: bromide (196 pm), chloride (181 pm), and fluoride (133 pm). In part because of its size, iodide forms relatively weak bonds with most elements. Computed Properties of 626-01-7.

Wu, Xiaofeng;Yang, Mengyao;Kim, Ji Seon;Wang, Rui;Kim, Gyoungmi;Ha, Jeongsun;Kim, Heejeong;Cho, Yejin;Nam, Ki Taek;Yoon, Juyoung research published 《 Reactivity Differences Enable ROS for Selective Ablation of Bacteria》, the research content is summarized as follows. An effective strategy to engineer selective photodynamic agents to surmount bacterial-infected diseases, especially Gram-pos. bacteria remains a great challenge. Herein, we developed two examples of compounds for a proof-of-concept study where reactive differences in reactive oxygen species (ROS) can induce selective ablation of Gram-pos. bacteria. Sulfur-replaced phenoxazinium (NBS-N) mainly generates a superoxide anion radical capable of selectively killing Gram-pos. bacteria, while selenium-substituted phenoxazinium (NBSe-N) has a higher generation of singlet oxygen that can kill both Gram-pos. and Gram-neg. bacteria. This difference was further evidenced by bacterial fluorescence imaging and morphol. changes. Moreover, NBS-N can also successfully heal the Gram-pos. bacteria-infected wounds in mice. We believe that such reactive differences may pave a general way to design selective photodynamic agents for ablating Gram-pos. bacteria-infected diseases.

Computed Properties of 626-01-7, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Iodide is one of the largest monatomic anions. It is assigned a radius of around 206 picometers. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline.For comparison, the lighter halides are considerably smaller: bromide (196 pm), chloride (181 pm), and fluoride (133 pm). In part because of its size, iodide forms relatively weak bonds with most elements. Synthetic Route of 626-01-7.

Xiang, Qiuping;Luo, Guolong;Zhang, Cheng;Hu, Qingqing;Wang, Chao;Wu, Tianbang;Xu, Hongrui;Hu, Jiankang;Zhuang, Xiaoxi;Zhang, Maofeng;Wu, Shuang;Xu, Jinxin;Zhang, Yan;Liu, Jinsong;Xu, Yong research published 《 Discovery, optimization and evaluation of 1-(indolin-1-yl)ethan-1-ones as novel selective TRIM24/BRPF1 bromodomain inhibitors》, the research content is summarized as follows. TRIM24 (tripartite motif-containing protein 24) and BRPF1 (bromodomain and PHD finger containing protein 1) are epigenetics “readers” and potential therapeutic targets for cancer and other diseases. Here we describe the structure-guided design of 1-(indolin-1-yl)ethan-1-ones as novel TRIM24/BRPF1 bromodomain inhibitors. The representative compound 20l (Y08624) is a new TRIM24/BRPF1 dual inhibitor, with IC50 values of 0.98 and 1.16 μM, resp. Cellular activity of 20l was validated by viability assay in prostate cancer (PC) cell lines. In PC xenograft models, 20l suppressed tumor growth (50 mg/kg/day, TGI = 53%) without exhibiting noticeable toxicity. Compound 20l represents a versatile starting point for the development of more potent TRIM24/BRPF1 inhibitors.

Synthetic Route of 626-01-7, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Organic iodides are used in veterinary products (Organic Iodide Powder) as a nutritional source of iodine. 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline. In the chemical industry, alkyl iodides serve as excellent alkylating agents and, specifically, methyl iodide is used as a methylating agent in the synthesis of various pharmaceutical drugs. HPLC of Formula: 626-01-7.

Yang, Rui;Du, Wenhao;Yuan, Huan;Qin, Tianhong;He, Renxiao;Ma, Yanni;Du, Haiying research published 《 Synthesis and biological evaluation of 2-phenyl-4-aminoquinolines as potential antifungal agents》, the research content is summarized as follows. A series of 4-aminoquinolines I [R = N,N-dimethylamino, anilino, 1,2,4-triazol-1-yl, etc.] were designed, synthesized and evaluated for their antifungal activities against three phytopathogenic fungi in-vitro. All of the target compounds I were fully elucidated by ¹H NMR, ¹³C NMR and HRMS spectra. The results indicated that most of the target compounds demonstrated significant activities against the tested fungi. Among them, compound I [R = 4-chloroanilino] exhibited more promising inhibitory activities against C. lunata (EC₅₀ = 13.3μg/mL), P. grisea (EC₅₀ = 14.4μg/mL) and A. alternate (EC₅₀ = 15.6μg/mL), superior to azoxystrobin, a com. agricultural fungicide. The structure-activity relationship (SAR) revealed that the aniline moiety at position 4 of the quinoline scaffold played a key role in the potency of a compound And the substitution positions of the aniline moiety significantly influenced the activities. These encouraging results yielded a variety of 2-phenylquinolines bearing an aniline moiety acting as promising antifungal agents.

626-01-7, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., HPLC of Formula: 626-01-7

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons-Smith reaction (cyclopropanation using iodomethane), 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline. Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction. Name: 3-Iodoaniline.

Wang, Yang;Zhang, Feng;Wang, Yi;Pan, Yi research published 《 Electrochemistry Enabled Nickel-Catalyzed Selective C-S Bond Coupling Reaction》, the research content is summarized as follows. This work describes an electrochem. enabled nickel-catalyzed chemoselective C-S bond coupling protocol for the production of aryl sulfides and sulfones. By simply switching the nickel catalysts and electrodes, this electrochem. C-S bond coupling has demonstrated excellent redox activity, scalability and sustainability. Furthermore, the mechanism for this electrochem. cross-coupling reaction has been investigated.

Name: 3-Iodoaniline, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Alkyl iodides react at a faster rate than alkyl fluorides due to the weak C-I bond. Iodo alkanes participate in a variety of organic synthesis reactions, which include the Simmons-Smith reaction (cyclopropanation using iodomethane), 626-01-7, formula is C6H6IN, Name is 3-Iodoaniline. Williamson ether synthesis, Wittig reaction, Grignard reaction, alkyl coupling reactions, and Wurtz reaction. Application of C6H6IN.

Wang, Ying;Chen, Ji-Kai;Xiong, Ling-Xiao;Wang, Bang-Jin;Xie, Sheng-Ming;Zhang, Jun-Hui;Yuan, Li-Ming research published 《 Preparation of Novel Chiral Stationary Phases Based on the Chiral Porous Organic Cage by Thiol-ene Click Chemistry for Enantioseparation in HPLC》, the research content is summarized as follows. Porous organic cages (POCs) are an emerging class of porous materials that have aroused considerable research interest because of their unique characteristics, including good solubility and a well-defined intrinsic cavity. However, there have so far been no reports of chiral POCs as chiral stationary phases (CSPs) for enantioseparation by high-performance liquid chromatog. (HPLC). Herein, we report the first immobilization of a chiral POC, NC1-R, on thiol-functionalized silica using a mild thiol-ene click reaction to prepare novel CSPs for HPLC. Two CSPs (CSP-1 and CSP-2) with different spacers have been prepared CSP-1, with a cationic imidazolium spacer, exhibited excellent enantioselectivity for the resolution of various racemates. Twenty-three and 12 racemic compounds or chiral drugs were well enantiosepd. on the CSP-1-packed column under normal-phase and reversed-phase conditions, resp., including alcs., diols, esters, ethers, ketones, epoxides, organic acids, and amines. In contrast, chiral resolution using CSP-2 (without a cationic imidazolium spacer)-packed column B was inferior to that of column A, demonstrating the important role of the cationic imidazolium spacer for chiral separation The chiral separation capability of column A was also compared with that of two most popular com. chiral columns, Chiralpak AD-H and Chiralcel OD-H, which exhibits good chiral recognition complementarity with the two com. chiral columns. In addition, five positional isomers dinitrobenzene, nitroaniline, chloroaniline, bromoaniline, and iodoaniline were also well separated on column A. The effects of temperature, mobile phase composition, and injected analyte mass for separation on column A were investigated. Column A also showed good stability and reproducibility after repeated injections. This work demonstrates that chiral POCs are promising chiral materials for HPLC enantioseparation

Application of C6H6IN, 3-Iodoaniline is a useful research compound. Its molecular formula is C6H6IN and its molecular weight is 219.02 g/mol. The purity is usually 95%.

3-Iodoaniline is a fatty acid that is used in analytical methods to measure the concentration of human serum in blood. It can be used to estimate the population growth rate, with a half-life of about 13 hours. 3-Iodoaniline reacts with hydrogen bond and proton to form a reaction solution, which can be catalyzed by palladium-catalyzed coupling and suzuki coupling reactions. The activation energies for these reactions are typically in the range of 4-8 kcal/mol. The chemical ionization technique is a type of mass spectrometry that is used to determine kinetic data for this compound. Hydrochloric acid can be added as an acid catalyst to increase the rate of reaction and generate more accurate kinetic data., 626-01-7.

Referemce:
Iodide – Wikipedia,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com