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197094-12-5

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197094-12-5 Usage

General Description

2-Methyl-3-(1H-pyrazol-1-yl)propanoic acid is a chemical compound with the molecular formula C9H12N2O2. It is a derivative of pyrazole and belongs to the class of organic compounds known as pyrazolopropionates. 2-METHYL-3-(1H-PYRAZOL-1-YL)PROPANOIC ACID is commonly used as a building block or intermediate in the synthesis of pharmaceuticals and other organic compounds. It has also been studied for its potential biological and pharmacological properties, including its anti-inflammatory and analgesic effects. However, further research is needed to fully understand its potential applications and mechanisms of action.

Check Digit Verification of cas no

The CAS Registry Mumber 197094-12-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,7,0,9 and 4 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 197094-12:
(8*1)+(7*9)+(6*7)+(5*0)+(4*9)+(3*4)+(2*1)+(1*2)=165
165 % 10 = 5
So 197094-12-5 is a valid CAS Registry Number.
InChI:InChI=1/C7H10N2O2/c1-6(7(10)11)5-9-4-2-3-8-9/h2-4,6H,5H2,1H3,(H,10,11)

197094-12-5 Well-known Company Product Price

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  • Aldrich

  • (CBR00373)  2-Methyl-3-(1H-pyrazol-1-yl)propanoic acid  AldrichCPR

  • 197094-12-5

  • CBR00373-1G

  • 1,930.50CNY

  • Detail

197094-12-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Methyl-3-(1H-pyrazol-1-yl)propanoic acid

1.2 Other means of identification

Product number -
Other names 2-methyl-3-pyrazol-1-ylpropanoic 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:197094-12-5 SDS

197094-12-5Upstream product

197094-12-5Downstream Products

197094-12-5Relevant articles and documents

Novel Parham-type Cycloacylations of 1H-Pyrazole-1-alkanoic Acids

Larsen, Scott D.

, p. 1013 - 1014 (2007/10/03)

Exposure of 1H-pyrazole-1-alkanoic acids to two equivalents of n-butyllithium affords the corresponding cyclic ketones via a Parham-type cyclization process. Although yields are modest, this procedure represents a simple and direct intramolecular acylation of a non-nucleophilic pyrazole carbon.

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