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3-Phenyl-1H-pyrrolo[2,3-c]pyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

25797-05-1

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25797-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 25797-05-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,7,9 and 7 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 25797-05:
(7*2)+(6*5)+(5*7)+(4*9)+(3*7)+(2*0)+(1*5)=141
141 % 10 = 1
So 25797-05-1 is a valid CAS Registry Number.

25797-05-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1H-pyrrolo[2,3-c]pyridine

1.2 Other means of identification

Product number -
Other names 3-Phenyl-1,6-diazainden

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:25797-05-1 SDS

25797-05-1Relevant academic research and scientific papers

Photoredox Cyanomethylation of Indoles: Catalyst Modification and Mechanism

O'Brien, Connor J.,Droege, Daniel G.,Jiu, Alexander Y.,Gandhi, Shivaani S.,Paras, Nick A.,Olson, Steven H.,Conrad, Jay

, p. 8926 - 8935 (2018/07/05)

The direct cyanomethylation of indoles at the 2- or 3-position was achieved via photoredox catalysis. The versatile nitrile synthon is introduced as a radical generated from bromoacetonitrile, a photocatalyst, and blue LED as a light source. The mechanism of the reaction is explored by determination of the Stern-Volmer quenching constants. By combining photophysical data and mass spectrometry to follow the catalyst decomposition, the catalyst ligands were tuned to enable synthetically useful yields of radical coupling products. A range of indole substrates with alkyl, aryl, halogen, ester, and ether functional groups participate in the reaction, affording products in 16-90% yields. The reaction allows the rapid construction of synthetically useful cyanomethylindoles, products that otherwise require several synthetic steps.

Vinylic MIDA boronates: New building blocks for the synthesis of aza-heterocycles

Llona-Minguez, Sabin,Desroses, Matthieu,Ghassemian, Artin,Jacques, Sylvain A.,Eriksson, Lars,Isacksson, Rebecka,Koolmeister, Tobias,Stenmark, P?l,Scobie, Martin,Helleday, Thomas

, p. 7394 - 7398 (2015/05/13)

Abstract A two-step synthesis of structurally diverse pyrrole-containing bicyclic systems is reported. ortho-Nitro-haloarenes coupled with vinylic N-methyliminodiacetic acid (MIDA) boronates generate ortho-vinyl-nitroarenes, which undergo a "metal-free" nitrene insertion, resulting in a new pyrrole ring. This novel synthetic approach has a wide substrate tolerance and it is applicable in the preparation of more complex "drug-like" molecules. Interestingly, an ortho-nitro-allylarene derivative furnished a cyclic β-aminophosphonate motif. Old dog, new tricks: A two-step synthesis of structurally diverse pyrrole-containing bicyclic systems is reported. ortho-Nitro-haloarenes coupled with vinylic N-methyliminodiacetic acid (MIDA) boronates generate ortho-vinyl-nitroarenes, which undergo a "metal-free" nitrene insertion, resulting in a new pyrrole ring. This approach has a wide substrate tolerance and it is applicable in the preparation of more complex "drug-like" molecules. Interestingly, an ortho-nitro-allylarene derivative furnished a cyclic β-aminophosphonate motif.

Palladium-catalyzed indole and azaindole synthesis by direct annulation of electron-poor o-chloroanilines and o-chloroaminopyridines with aldehydes

Xu, Zhengren,Hu, Weimin,Zhang, Fengying,Li, Qingjiang,Lue, Zhiyao,Zhang, Lihe,Jia, Yanxing

experimental part, p. 3981 - 3987 (2009/05/27)

A practical process for the synthesis of 2-unsubstituted indoles and azaindoles has been developed by the palladium-catalyzed direct annulation of electron-poor o-chloro/bromoanilines and o-chloroaminopyridines with aldehydes. Coupled with the previous results of Jia and Zhu, this allows rapid access to a variety of 2-unsubstituted indoles and azaindoles starting from simple and easily accessible precursors. Georg Thieme Verlag Stuttgart.

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