Category: 606-55-3

Boev, V. I. published the artcile2- And 4-methylmercurated quinolinium salts, Application of 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Zhurnal Obshchei Khimii (1994), 64(7), 1128-33, database is CAplus.

Mercuration of 2- and 4-methylquinolinium salts with HgX₂ (X = OAc, O₂CCF₃) gave the corresponding mono-, di-, and trimethylmercurated quinolinium salts depending on the ratio of reactants. Some reactions of these salts are reported with CaCl₂, KI, NaOH, and Br₂ in HOAc.

Zhurnal Obshchei Khimii published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Application of 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Heald, Robert A. published the artcileAntitumor polycyclic acridines. 8.Synthesis and telomerase-inhibitory activity of methylated pentacyclic acridinium salts, Product Details of C12H14IN, the publication is Journal of Medicinal Chemistry (2002), 45(3), 590-597, database is CAplus and MEDLINE.

Two short routes to novel methylated pentacyclic quinoacridinium salts have been devised. New compounds display telomerase-inhibitory potency (<1 μM) in the TRAP assay. 3,11-Difluoro-6,8,13-trimethyl-8H-quino[4,3,2-kl]acridinium methosulfate ( RHPS4, NSC 714187) has a higher selectivity for triplex and quadruplex DNA structures than the 3,6,8,11,13-pentamethyl analog (RHPS3, NSC 714186) and a low overall growth-inhibitory activity in the NCI 60 cell panel (mean GI₅₀ 13.18 μM); in addition, the activity profile of NSC 714187 does not COMPARE with agents of the topoisomerase II class. Compound NSC 714187 is soluble in water, stable in the pH range of 5-9, efficiently transported into tumor cells, and is currently the lead structure for further elaboration in this new class of telomerase inhibitor.

Journal of Medicinal Chemistry published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Product Details of C12H14IN.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Feng, Huan published the artcileResponsive Fluorescence Probe for Selective and Sensitive Detection of Hypochlorous Acid in Live Cells and Animals, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Chemistry – An Asian Journal (2018), 13(18), 2611-2618, database is CAplus and MEDLINE.

The development of effective bioanal. methods for rapid, sensitive and specific detection of HOCl in vitro and in vivo plays a key role for better understanding the roles of this mol. in normal and diseased conditions, but remains challenging due to the highly reactive nature of HOCl and the complicated biol. conditions. A new fluorescence probe, PQI(I), was developed for monitoring of the HOCl level in biol. samples. PQI was easily synthesized by a one-step condensation reaction. Upon addition of HOCl, significant changes in the absorption spectra and the color of the solution were noticed, facilitating the “naked eye” detection of HOCl in PBS buffer. The fluorescence of PQI is significantly increased within a few seconds, leading to “OFF-ON” fluorescence response towards HOCl. The sensing mechanism, oxidation of thioether by HOCl, was confirmed by HRMS titration anal. PQI features a large Stokes shift, high sensitivity and selectivity, and rapid fluorescence response towards HOCl. Quant. detection of HOCl in single live cells was demonstrated through fluorescence imaging and flow cytometry anal. PQI was then successfully used in visualization of HOCl in live zebrafish and nude mice.

Chemistry – An Asian Journal published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Hammond, David M. published the artcileDNA photography: an ultrasensitive DNA-detection method based on photographic techniques, Product Details of C12H14IN, the publication is Angewandte Chemie, International Edition (2007), 46(22), 4184-4187, database is CAplus and MEDLINE.

All there in black and white: DNA labeled with spectral sensitizers applied to com. available photopaper allows the detection of oligonucleotides with extreme sensitivity. The detection of the DNA with the help of black and white photog. is shown in the picture (ODN = oligodeoxyribonucleotide).

Angewandte Chemie, International Edition published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Product Details of C12H14IN.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Wang, Yan published the artcileEnantioselective Rhodium-Catalyzed Dearomative Arylation or Alkenylation of Quinolinium Salts, Application of 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Angewandte Chemie, International Edition (2016), 55(11), 3776-3780, database is CAplus and MEDLINE.

A highly enantioselective rhodium(I)-catalyzed dearomative arylation or alkenylation of easily available N-alkylquinolinium salts is reported, thus providing an effective and practical approach to the synthesis of dihydroquinolines in up to 99% ee. This reaction tolerates a wide range of functional groups with respect to both the organic boronic acids and the quinoline starting materials. Moreover, the synthetic utility of this protocol is demonstrated in the formal asym. synthesis of bioactive tetrahydroquinoline and the total syntheses of (-)-angustureine and (+)-cuspareine.

Angewandte Chemie, International Edition published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C15H21BO3, Application of 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Lugovskii, A. P. published the artcileSynthesis and photodynamic effect of meso-substituted tricarbocyanine dyes with ortho-phenylene bridge in chromophore chain, SDS of cas: 606-55-3, the publication is Vestnik BGU, Seriya 2: Khimiya, Biologiya, Geografiya (2011), 14-18, database is CAplus.

Meso-chlorine and meso-fluorine substituted tricarbocyanine dyes with ortho-phenylene bridge in the chromophore are synthesized. The replacement of meso-chlorine to meso-fluorine in polyene system of synthon of the received dyes is investigated. A number of the synthesized substances have shown high photodynamic activity in vitro.

Vestnik BGU, Seriya 2: Khimiya, Biologiya, Geografiya published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, SDS of cas: 606-55-3.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Antonious, Maged S. published the artcileSolvent polarity indicators: mass spectral properties of some styryl pyridinium and quinolinium salts, Product Details of C12H14IN, the publication is Annali di Chimica (Rome, Italy) (1993), 83(9-10), 457-60, database is CAplus.

I (R = H, RR = CH:CHCH:CH; R¹ = H, NMe₂, NO₂) were prepared by reaction of 2-methylpyridinium ethiodide or quinaldinium ethiodide with the corresponding benzaldehyde derivative The fragmentation pathways of I during mass spectrometry were studied.

Annali di Chimica (Rome, Italy) published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Product Details of C12H14IN.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Lugovskii, A. P. published the artcileSynthesis and photodynamic effect of meso-substituted tricarbocyanine dyes with ortho-phenylene bridge in chromophore chain, SDS of cas: 606-55-3, the publication is Vestnik BGU, Seriya 2: Khimiya, Biologiya, Geografiya (2011), 14-18, database is CAplus.

Meso-chlorine and meso-fluorine substituted tricarbocyanine dyes with ortho-phenylene bridge in the chromophore are synthesized. The replacement of meso-chlorine to meso-fluorine in polyene system of synthon of the received dyes is investigated. A number of the synthesized substances have shown high photodynamic activity in vitro.

Vestnik BGU, Seriya 2: Khimiya, Biologiya, Geografiya published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, SDS of cas: 606-55-3.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Wang, Yan published the artcileEnantioselective Rhodium-Catalyzed Dearomative Arylation or Alkenylation of Quinolinium Salts, Application of 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Angewandte Chemie, International Edition (2016), 55(11), 3776-3780, database is CAplus and MEDLINE.

A highly enantioselective rhodium(I)-catalyzed dearomative arylation or alkenylation of easily available N-alkylquinolinium salts is reported, thus providing an effective and practical approach to the synthesis of dihydroquinolines in up to 99% ee. This reaction tolerates a wide range of functional groups with respect to both the organic boronic acids and the quinoline starting materials. Moreover, the synthetic utility of this protocol is demonstrated in the formal asym. synthesis of bioactive tetrahydroquinoline and the total syntheses of (-)-angustureine and (+)-cuspareine.

Angewandte Chemie, International Edition published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C15H21BO3, Application of 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Tan, Li published the artcileA coumarin-quinolinium-based fluorescent probe for ratiometric sensing of sulfite in living cells, Related Products of iodides-buliding-blocks, the publication is Organic & Biomolecular Chemistry (2014), 12(26), 4637-4643, database is CAplus and MEDLINE.

Based on a novel coumarin-quinolinium platform, probe 2 was rationally designed and synthesized as a novel ratiometric fluorescent sensor for sulfite anions. The probe exhibited a wide dynamic concentration range for sulfite anions in a PBS buffer (containing 1 mg mL^-1 BSA). More importantly, the probe was suitable for ratiometric fluorescence imaging in living cells with high sensitivity, favorable selectivity, and minimal cytotoxicity.

Organic & Biomolecular Chemistry published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C13H10F2, Related Products of iodides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com