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902131-33-3

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902131-33-3 Usage

General Description

2-(1H-indazol-4-yl)acetic acid is a chemical compound with a molecular formula C11H9N3O2. It belongs to the class of organic compounds known as indazoles, which are polycyclic aromatic compounds containing an indazole moiety, a bicyclic compound consisting of a benzene ring fused to a five-membered nitrogen-containing ring. 2-(1H-indazol-4-yl)acetic acid is used in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical drugs. Its potential therapeutic applications include anticancer, anti-inflammatory, and antimicrobial properties. The compound is an organic acid and contains a carboxylic acid functional group, which makes it a versatile building block for the synthesis of other chemical compounds. Overall, 2-(1H-indazol-4-yl)acetic acid has diverse potential applications in drug discovery and development due to its unique chemical structure and properties.

Check Digit Verification of cas no

The CAS Registry Mumber 902131-33-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,0,2,1,3 and 1 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 902131-33:
(8*9)+(7*0)+(6*2)+(5*1)+(4*3)+(3*1)+(2*3)+(1*3)=113
113 % 10 = 3
So 902131-33-3 is a valid CAS Registry Number.

902131-33-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(1H-indazol-4-yl)acetic acid

1.2 Other means of identification

Product number -
Other names (1H-indazol-4-yl)acetic 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:902131-33-3 SDS

902131-33-3Downstream Products

902131-33-3Relevant articles and documents

Synthesis of 8-substituted-6-phenyl-6,7,8,9-tetrahydro-3H-pyrazolo[4,3-f]isoquinolines using Pictet-Spengler and Bischler-Napieralski cyclisation methods

Davies, Robert D.M.,Pink, Jennifer H.,Scott, James S.,Bailey, Andrew

, p. 2917 - 2920 (2018)

In the following communication we report routes for the synthesis of a set of 8-substituted-6-phenyl-6,7,8,9-tetrahydro-3H-pyrazolo[4,3-f]isoquinolines. Pictet-Spengler and Bischler-Napieralski methodologies were employed on the relevant indazole precursors and the merits of the two cyclisation reactions for preparing these structures were assessed.

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