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22072-89-5

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22072-89-5 Usage

Synthesis Reference(s)

Journal of Heterocyclic Chemistry, 10, p. 883, 1973 DOI: 10.1002/jhet.5570100538

Check Digit Verification of cas no

The CAS Registry Mumber 22072-89-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,0,7 and 2 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22072-89:
(7*2)+(6*2)+(5*0)+(4*7)+(3*2)+(2*8)+(1*9)=85
85 % 10 = 5
So 22072-89-5 is a valid CAS Registry Number.

22072-89-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-chloro-3-phenyl-1H-indole

1.2 Other means of identification

Product number -
Other names 5-Cl-3-Ph-indole

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:22072-89-5 SDS

22072-89-5Relevant articles and documents

Ir(iii)-Catalysed electrooxidative intramolecular dehydrogenative C-H/N-H coupling for the synthesis of N-H indoles

Chang, Sukbok,Kim, Dongwook,Kim, Youyoung

, p. 12309 - 12312 (2021/12/07)

Herein, an iridium(iii)-catalysed electrooxidative intramolecular dehydrogenative C-H/N-H coupling of unprotected 2-alkenyl anilines is described. The developed method allows the synthesis of a variety of 3-substituted N-H indole scaffolds under undivided electrolytic conditions. Mechanistic studies suggest that the reaction proceeds through the electro-oxidation induced reductive elimination pathway.

Synthesis and antimycobacterial activity of 3-phenyl-1h-indoles

Abbadi, Bruno Lopes,Basso, Luiz Augusto,Bizarro, Cristiano Valim,Dornelles, Maiele,Duarte, Lovaine,Etchart, Renata Jardim,Lourega, Rogério Vescia,Macchi, Fernanda Souza,Machado, Pablo,Neves, Christiano Ev,Perelló, Marcia Alberton,Rambo, Raoní S.,Silva, Fernanda Fries,Sperotto, Nathalia

, (2021/08/31)

Tuberculosis has been described as a global health crisis since the 1990s, with an estimated 1.4 million deaths in the last year. Herein, a series of 20 1H-indoles were synthesized and evaluated as in vitro inhibitors of Mycobacterium tuberculosis (Mtb) g

Metal-free and regiospecific synthesis of 3-arylindoles

Xie, Wenlai,Xu, Chuangchuang,Xu, Jiaxi

, p. 2661 - 2671 (2020/04/17)

A convenient, metal-free, and organic acid-base promoted synthetic method to prepare 3-arylindoles from 3-aryloxirane-2-carbonitriles and arylhydrazine hydrochlorides has been developed. In the reaction, the organic acid catalyzes a tandem nucleophilic ri

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