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896722-50-2

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896722-50-2 Usage

Description

1H-Pyrrolo[2,3-b]pyridine, 6-chloro-1-(phenylsulfonyl)is a chemical compound that belongs to the pyrrolopyridine class. It features a pyridine ring fused to a pyrrole ring, with a chlorine atom and a phenylsulfonyl group attached to it. 1H-Pyrrolo[2,3-b]pyridine, 6-chloro-1-(phenylsulfonyl)possesses potential biological and pharmacological activities, making it valuable in scientific research and drug development. Its properties and behavior in various environments are of interest to chemists and researchers, and it may have applications in treating a range of diseases and conditions.

Uses

Used in Pharmaceutical Industry:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-1-(phenylsulfonyl)is used as a pharmaceutical intermediate for the development of new drugs. Its unique structure and potential biological activities make it a promising candidate for the treatment of various diseases and conditions.
Used in Scientific Research:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-1-(phenylsulfonyl)is used as a research compound to study its properties, behavior, and interactions with other molecules. This helps researchers gain insights into its potential applications and optimize its use in various fields.
Used in Chemical Synthesis:
1H-Pyrrolo[2,3-b]pyridine, 6-chloro-1-(phenylsulfonyl)can be used as a building block in the synthesis of more complex molecules and compounds. Its unique structure and functional groups make it a versatile component in the development of new chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 896722-50-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,6,7,2 and 2 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 896722-50:
(8*8)+(7*9)+(6*6)+(5*7)+(4*2)+(3*2)+(2*5)+(1*0)=222
222 % 10 = 2
So 896722-50-2 is a valid CAS Registry Number.
InChI:InChI=1/C13H9ClN2O2S/c14-12-7-6-10-8-9-16(13(10)15-12)19(17,18)11-4-2-1-3-5-11/h1-9H

896722-50-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(benzenesulfonyl)-6-chloropyrrolo[2,3-b]pyridine

1.2 Other means of identification

Product number -
Other names 1-benzenesulfonyl-6-chloro-1H-pyrrolo[2,3-b]pyridine

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:896722-50-2 SDS

896722-50-2Relevant articles and documents

N-(PHENYL)-INDOLE-3-SULFONAMIDE DERIVATIVES AND RELATED COMPOUNDS AS GPR17 MODULATORS FOR TREATING CNS DISORDERS SUCH AS MULTIPLE SCLEROSIS

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Page/Page column 63, (2021/01/22)

Disclosed are N-(phenyl)-lH-indole-3-sulfonamide and N-(phenyl) -1 H-pyrrolo[2,3-b]pyridine-3-sulfonamide derivatives of formula I substituted at the 1- and 6-positions of the 1H-indole or 1H-pyrrolo[2,3-b]pyridine moiety, as well as structurally related

PYRIDINYL AND PYRAZINYL-(AZA)INDOLSULFONAMIDES

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Page/Page column 92; 94-95, (2020/01/11)

The present invention relates to pyridinyl and pyrazinyl-(aza)indolsulfonamides having GPR17 modulator activity. The compounds have utility in the treatment of a variety of GPR17-associated disorders.

Scaffold-hopping strategy: Synthesis and biological evaluation of 5,6-fused bicyclic heteroaromatics to identify orally bioavailable anticancer agents

Tung, Yen-Shih,Coumar, Mohane Selvaraj,Wu, Yu-Shan,Shiao, Hui-Yi,Chang, Jang-Yang,Liou, Jing-Ping,Shukla, Paritosh,Chang, Chun-Wei,Chang, Chi-Yen,Kuo, Ching-Chuan,Yeh, Teng-Kuang,Lin, Chin-Yu,Wu, Jian-Sung,Wu, Su-Ying,Liao, Chun-Chen,Hsieh, Hsing-Pang

, p. 3076 - 3080 (2011/06/25)

Utilizing scaffold-hopping drug-design strategy, we sought to identify a backup drug candidate for BPR0L075 (1), an indole-based anticancer agent. For this purpose, 5,6-fused bicyclic heteroaromatic scaffolds were designed and synthesized through shufflin

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