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1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester is a significant heterocyclic chemical compound, characterized by a pyrrolopyridine core and a phenylsulfonyl group. It is a methyl ester derivative of the parent carboxylic acid, which has garnered attention for its potential pharmaceutical applications, particularly in the treatment of diseases such as cancer and inflammatory disorders.

245064-81-7

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245064-81-7 Usage

Uses

Used in Pharmaceutical Industry:
1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester is used as a potential therapeutic agent for the treatment of certain diseases and conditions. Its unique structure and pharmacological properties make it a promising candidate for drug development, with potential applications in the management of cancer and inflammatory disorders.
1-(Phenylsulfonyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester's heterocyclic nature and functional groups may contribute to its ability to modulate biological targets and pathways involved in disease processes. Its potential as a treatment option is currently under investigation, with researchers and pharmaceutical companies exploring its efficacy and safety in preclinical and clinical studies.
In Drug Development:
1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester is used as a lead compound in the discovery and optimization of new drugs. Its chemical structure can be modified to improve its pharmacokinetic and pharmacodynamic properties, enhancing its potential as a therapeutic agent. 1-(Phenylsulfonyl)-1h-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester's versatility and the possibility of structural modifications make it an attractive starting point for the development of novel drugs with improved efficacy and selectivity.
In Medicinal Chemistry Research:
1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester is used as a research tool in medicinal chemistry to study the structure-activity relationships of heterocyclic compounds. Understanding how its chemical features influence biological activity can provide valuable insights into the design of more effective and selective drugs.
In addition to its potential therapeutic applications, 1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester may also find use in other areas of pharmaceutical research, such as the development of diagnostic agents, imaging agents, or as chemical probes to study biological processes.
Overall, the diverse applications of 1-(Phenylsulfonyl)-1H-pyrrolo[2,3-b]pyridine-3-carboxylic acid methyl ester highlight its importance in the field of pharmaceutical chemistry and its potential to contribute to the development of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 245064-81-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,0,6 and 4 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 245064-81:
(8*2)+(7*4)+(6*5)+(5*0)+(4*6)+(3*4)+(2*8)+(1*1)=127
127 % 10 = 7
So 245064-81-7 is a valid CAS Registry Number.

245064-81-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name methyl 1-(benzenesulfonyl)pyrrolo[2,3-b]pyridine-3-carboxylate

1.2 Other means of identification

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

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:245064-81-7 SDS

245064-81-7Relevant academic research and scientific papers

Synthesis of benzo[5',6']cyclohepta[4,5]pyrrolo[2,3-b]pyridin-12-one

Mouaddib, Abderrahim,Joseph, Benoit,Hasnaoui, Aissa,Merour, Jean-Yves

, p. 5853 - 5854 (2007/10/03)

The synthesis of a 7-azaindole derivative 8 with potential antitumoral activity is described starting from pyrrolo[2,3-b]pyridine; regioselective lithiation/methylation of alkyl 7-azaindole-3-carboxylates 4 afforded the 2- methyl derivatives 5. Demethylat

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