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1-Benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid is a chemical compound characterized by the molecular formula C19H12N2O4S. It is a derivative of pyrrolopyridine and carboxylic acid, featuring a benzenesulfonyl group attached to the pyrrolopyridine ring and a carboxylic acid group. 1-Benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid is recognized for its potential applications in the pharmaceutical industry, particularly as an intermediate in the synthesis of various organic compounds and pharmaceuticals.

189089-90-5

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189089-90-5 Usage

Uses

Used in Pharmaceutical Industry:
1-Benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid is used as a key intermediate in the synthesis of pharmaceutical compounds, specifically for the development of potential anti-cancer and anti-inflammatory drugs. Its unique molecular structure and functional groups make it a valuable building block in the creation of diverse organic compounds and pharmaceuticals, contributing to the advancement of novel therapeutic agents.
Used in Organic Synthesis:
1-Benzenesulfonyl-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid is employed as a versatile building block in organic synthesis, allowing for the construction of a wide range of chemical entities. Its presence in the synthesis process can lead to the development of new compounds with potential applications in various fields, such as materials science, agrochemistry, and specialty chemicals.

Check Digit Verification of cas no

The CAS Registry Mumber 189089-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,9,0,8 and 9 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 189089-90:
(8*1)+(7*8)+(6*9)+(5*0)+(4*8)+(3*9)+(2*9)+(1*0)=195
195 % 10 = 5
So 189089-90-5 is a valid CAS Registry Number.
InChI:InChI=1/C14H10N2O4S/c17-14(18)12-9-10-5-4-8-15-13(10)16(12)21(19,20)11-6-2-1-3-7-11/h1-9H,(H,17,18)

189089-90-5SDS

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 1-(benzenesulfonyl)pyrrolo[2,3-b]pyridine-2-carboxylic acid

1.2 Other means of identification

Product number -
Other names 1-(phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-2-carboxylic acid

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:189089-90-5 SDS

189089-90-5Relevant articles and documents

Synthesis, biological evaluation and molecular modeling of a novel series of 7-azaindole based tri-heterocyclic compounds as potent CDK2/Cyclin E inhibitors

Baltus, Christine B.,Jorda, Radek,Marot, Christophe,Berka, Karel,Bazgier, Václav,Kry?tof, Vladimír,Prié, Gildas,Viaud-Massuard, Marie-Claude

, p. 701 - 719 (2016/01/09)

From four molecules, inspired by the structural features of fascaplysin, with an interesting potential to inhibit cyclin-dependent kinases (CDKs), we designed a new series of tri-heterocyclic derivatives based on 1H-pyrrolo[2,3-b]pyridine (7-azaindole) an

Design, synthesis and biological evaluation of new thalidomide analogues as TNF-α and IL-6 production inhibitors

Chaulet, Charlotte,Croix, Cécile,Alagille, David,Normand, Sylvain,Delwail, Adriana,Favot, Laure,Lecron, Jean-Claude,Viaud-Massuard, Marie-Claude

, p. 1019 - 1022 (2011/03/21)

Several thalidomide analogues were synthesized and compared to thalidomide and its more active analogue, lenalidomide, for their ability to inhibit the production of the pro-inflammatory cytokine tumour necrosis factor (TNF)-α and interleukin (IL)-6 by LPS-activated peripheral blood mononuclear cells (PBMCs). Among these compounds, two analogues containing sulfonyl group displayed interesting downregulation of TNF-α and IL-6 production.

AZAINDOLE CARBOXAMIDES

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Page/Page column 30, (2010/11/30)

The invention relates to azaindole derivatives of general formula (I), wherein X represents a group of general formula (X1). Said compounds have a therapeutic potential in the treatment of diseases that are accompanied by an impaired dopamine metabolism a

Synthesis of 2-substituted-1H-pyrrolo[2,3-b]pyridines: Preparation of 7-azaolivacine analogue and 7-azaindolopyridopyrimidine derivatives

Desarbre, Eric,Coudret, Sandrine,Meheust, Cecile,Merour, Jean-Yves

, p. 3637 - 3648 (2007/10/03)

2-Substituted-1H-pyrrolo(2,3-b]pyridines have been prepared from 7-azaindole by lithiation followed by addition of various electrophiles. A 7-azaolivacine analogue and pyrido[3'2':4,5]pyrrolo[1,2-c]pyrido[3,2-d]pyrimidine have also been prepared.

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