Category: 21969-05-1

Correlation between molecular dipole moment and centrosymmetry in some crystalline diphenyl ethers was written by Dey, Archan;Desiraju, Gautam R.. And the article was included in Chemical Communications (Cambridge, United Kingdom) in 2005.Synthetic Route of C12H8INO3 The following contents are mentioned in the article:

The presence of a large mol. dipole moment in di-Ph ethers leads unequivocally to a centrosym. crystal structure. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Synthetic Route of C12H8INO3).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole, also called Benzopyrrole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter. In addition to indole, the strain-release chemistry worked for numerous substrates including amines, alcohols, thiols, carboxylic acids, imidazoles, and pyrazoles.Synthetic Route of C12H8INO3

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

CuI Nanoparticles for C-N and C-O Cross Coupling of Heterocyclic Amines and Phenols with Chlorobenzenes was written by Sreedhar, B.;Arundhathi, R.;Reddy, P. Linga;Kantam, M. Lakshmi. And the article was included in Journal of Organic Chemistry in 2009.Application of 21969-05-1 The following contents are mentioned in the article:

Employing CuI nanoparticles as an efficient catalyst for the cross-coupling reactions of various N/O nucleophilic reagents with aryl chlorides could be successfully carried out under mild conditions in the absence of both the ligands and strong bases. A variety of products including N-arylimidazoles and aryl ethers were synthesized in good to excellent yields. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Application of 21969-05-1).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole, first isolated in 1866, and it is commonly synthesized from phenylhydrazine and pyruvic acid, although several other procedures have been discovered. It is used in perfumery and in making tryptophan, an essential amino acid, and indoleacetic acid (heteroauxin), a hormone that promotes the development of roots in plant cuttings.Application of 21969-05-1

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

Nitrodiphenyl ethers from 1,2- or 1,4-dinitrobenzenes and copper in pyridine was written by Bjorklund, Christer;Wahren, Robert. And the article was included in Acta Chemica Scandinavica in 1976.Computed Properties of C12H8INO3 The following contents are mentioned in the article:

Reaction of o-C6H4(NO2)2 (I) with Cu in pyridine at 116掳 gave 65% (o-O2NC6H4)2O (II); 77% (p-O2NC6H4)2O was obtained from p-C6H4(NO2)2 similarly. Treatment of I with Cu in pyridine and BuX (X = I, Br, Cl) gave o-BuOC6H4NO2, II, and o-O2NC6H4OH (III). Reaction of the dinitrobenzenes, Cu, and phenols in boiling pyridine gave unsym. diaryl ether, sym. diaryl ether and III. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Computed Properties of C12H8INO3).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. More than 200 indole derivatives have already been marketed as drugs or are under advanced stages of clinical trials.Computed Properties of C12H8INO3

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

Trifluoromethylthiolation of Unsymmetrical 位³-Iodane Derivatives: Additive-Free, Selective and Scalable Introduction of the SCF₃ Group was written by Nikolaienko, Pavlo;Yildiz, Tuelay;Rueping, Magnus. And the article was included in European Journal of Organic Chemistry in 2016.Recommanded Product: 1-Iodo-4-(4-nitrophenoxy)benzene The following contents are mentioned in the article:

The reaction of copper trifluoromethyl sulfide with diaryliodonium salts provides a straightforward pathway for the synthesis of aryl trifluoromethyl thioethers under mild reaction conditions and within short reaction times. High chemoselectivity was achieved by using mesityl as a leaving group. A large range of novel [(het)aryl](mesityl)iodonium salts underwent this reaction under the optimized conditions to give the desired products in moderate to good yields. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Recommanded Product: 1-Iodo-4-(4-nitrophenoxy)benzene).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. More than 200 indole derivatives have already been marketed as drugs or are under advanced stages of clinical trials.Recommanded Product: 1-Iodo-4-(4-nitrophenoxy)benzene

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

CsF/clinoptilolite: an efficient solid base in S_NAr and copper-catalyzed Ullmann reactions was written by Keipour, Hoda;Hosseini, Abolfazl;Afsari, Amir;Oladee, Razieh;Khalilzadeh, Mohammad A.;Ollevier, Thierry. And the article was included in Canadian Journal of Chemistry in 2016.Application In Synthesis of 1-Iodo-4-(4-nitrophenoxy)benzene The following contents are mentioned in the article:

CsF/clinoptilolite was found to be an efficient solid base catalyst for both S_NAr and Ullmann ether reactions. A general and efficient one-step procedure was developed for the synthesis of biaryl ethers via direct coupling of electron-deficient aryl halides to phenols using CsF/clinoptilolite. The protocol was also applied to electron-rich aryl halides by addition of a catalytic amount of copper oxide nanoparticles. Both S_NAr and Ullmann reactions were rapid and provided good to excellent yields. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Application In Synthesis of 1-Iodo-4-(4-nitrophenoxy)benzene).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole, also called Benzopyrrole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter. More than 200 indole derivatives have already been marketed as drugs or are under advanced stages of clinical trials.Application In Synthesis of 1-Iodo-4-(4-nitrophenoxy)benzene

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

Ligand-free solid supported palladium(0) nano/microparticles promoted C-O, C-S, and C-N cross coupling reaction was written by Bandna;Guha, Nitul Ranjan;Shil, Arun K.;Sharma, Dharminder;Das, Pralay. And the article was included in Tetrahedron Letters in 2012.Name: 1-Iodo-4-(4-nitrophenoxy)benzene The following contents are mentioned in the article:

Ligand-free solid-supported nano and microparticles of Pd(0) (SS-Pd) were used as a heterogeneous catalyst in carbon-heteroatom bond formation reactions. Nitro substituted aryl halides reacted with oxygen, sulfur, and nitrogen nucleophiles to afford the corresponding products in good yields. A one-pot sequential cross coupling and nitro-reduction was also performed using the same SS-Pd catalyst to access amine substituted carbon-heteroat. mols. In addition, SS-Pd could be recycled up to seven runs without a significant loss of catalytic activity. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Name: 1-Iodo-4-(4-nitrophenoxy)benzene).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. The indole subunit is an almost ubiquitous component of biologically active natural products, and its study has been the focus of research for decades. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Name: 1-Iodo-4-(4-nitrophenoxy)benzene

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

Interaction of functional groups through π-electron systems. V. Interaction through aromatic rings connected by a monofunctional bridging group was written by Lutskii, A. E.;Obukhova, E. M.;Cheshko, R. S.. And the article was included in Zhurnal Fizicheskoi Khimii in 1968.Application of 21969-05-1 The following contents are mentioned in the article:

Dipole moments (μH) of 4-XC6H4ZC6H4Y-4′ where Z was CH2, O, S, NH, and CH2CH2 and X and Y were NO2, CN, Cl, Br, I, OH, Me, and NH2 were measured. Values of μH prove existence of the interaction of the substituents in 4,4′ position through bridges with σ and p electrons. Any change in the electron d. at Z in the case of its interaction with substituents of the 1st ring causes a change in degree of its interaction with substituents of the 2nd ring. Only electron effects are transmitted from one substituent to the other substituents of the rings through the bridging groups. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Application of 21969-05-1).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole, also called Benzopyrrole, a heterocyclic organic compound occurring in some flower oils, such as jasmine and orange blossom, in coal tar, and in fecal matter. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Application of 21969-05-1

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

QSAR of nitro-diphenylethers as inhibitors of cyclic photophosphorylation was written by Oettmeier, Walter;Masson, Klaus;Donner, Andreas. And the article was included in Zeitschrift fuer Naturforschung in 1988.Quality Control of 1-Iodo-4-(4-nitrophenoxy)benzene The following contents are mentioned in the article:

Twenty-five nitro-diphenylethers were synthesized and assayed for their inhibitory activity in N-methylphenazonium-methosulfate-mediated cyclic photophosphorylation. Their pI₅₀-values ranged 3.5-5.3. A QSAR-anal. revealed that the lipophilicity of the nitro-diphenylethers as expressed by ∑π played a major role. In addition, the Taft steric parameter E_s in positions 6′, 4′ and 2′ (in decreasing order) contributed to the inhibitory activity. For maximal biol. activity, positions 4′ and 6′ should be left unsubstituted, whereas a bulky substituent is required for position 2′. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Quality Control of 1-Iodo-4-(4-nitrophenoxy)benzene).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole exists overwhelmingly in the 1H-indole form as do other simple indoles.Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Quality Control of 1-Iodo-4-(4-nitrophenoxy)benzene

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

Palladium-Catalyzed Formation of Poly(imide-amides). 1. Reactions with Diiodo Imides and Diamines was written by Perry, Robert J.;Turner, S. Richard;Blevins, Richard W.. And the article was included in Macromolecules in 1994.Formula: C12H8INO3 The following contents are mentioned in the article:

High-mol.-weight poly(imide-amides) can be readily formed by the Pa-mediated carbonylation and condensation reactions of diiodo imide monomers and aromatic diamines. Reaction conditions for polymerization are 100-120°, 90 psig CO, 3-6% PdCl₂L₂ (L = PPh₃), and 2.4 equiv of DBU (1,8-diazabicyclo[5.4.0]undec-7-ene) for 2-4 h in DMAc or NMP. This route offers the flexibility of incorporating different ratios of amide and imide groups in the polymer backbone in a controlled manner. The imide moiety is preformed, which eliminates the possibility of postpolymn. curing. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Formula: C12H8INO3).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole could be stereoselectively alkylated with chiral cyclopentyl sulfone reagent. Indole was synthesized in moderate yield via an o-naphthoquinone catalyzed tandem cross-coupling of substituted aniline and benzylamine under aerobic oxidation conditions.Formula: C12H8INO3

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

Cellulose nanocrystals-palladium, a novel recyclable catalyst for coupling reaction was written by Seyednejhad, Sajedeh;Khalilzadeh, Mohammad A.;Sadeghifar, Hasan;Zareyee, Daryoush. And the article was included in Eurasian Chemical Communications in 2020.Synthetic Route of C12H8INO3 The following contents are mentioned in the article:

A new Schiff base catalyst (Pd(II) chem. mounted on the cellulose nanocrystals surface) was developed for Ullmann and Suzuki cross-coupling reactions. The catalyst was applied to the Ullmann reaction using a series of aryl halides and phenol derivatives in DMSO. The Suzuki cross-coupling reaction of aryl halides and phenylboronic acids gave biaryl compounds The catalyst was characterized by FTIR, XRD, SEM, ICP-AES and TGA techniques and demonstrated high reaction efficiency with more than 90% reaction yield. The catalyst could also be recovered and used several times and demonstrated good performance. This study involved multiple reactions and reactants, such as 1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1Synthetic Route of C12H8INO3).

1-Iodo-4-(4-nitrophenoxy)benzene (cas: 21969-05-1) belongs to iodide derivatives. Indole produced by Proteus, Pseudomonas, Escherichia and other species was shown to be a growth promoting factor in Arabidopsis thaliana. They are capable of binding to a variety of receptors with high affinity and thus have applications in a wide range of therapeutic areas.Synthetic Route of C12H8INO3

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