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1H-Pyrazole-3-carboxylic acid, 5-methyl-, 2-(2-chloro-6-methylphenyl)hydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

89270-46-2

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89270-46-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89270-46-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,7 and 0 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 89270-46:
(7*8)+(6*9)+(5*2)+(4*7)+(3*0)+(2*4)+(1*6)=162
162 % 10 = 2
So 89270-46-2 is a valid CAS Registry Number.

89270-46-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methyl-2H-pyrazole-3-carboxylic acid N'-(2-chloro-6-methyl-phenyl)-hydrazide

1.2 Other means of identification

Product number -
Other names -

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:89270-46-2 SDS

89270-46-2Downstream Products

89270-46-2Relevant academic research and scientific papers

Pyrazolecarboxylic acid hydrazides as antiinflammatory agents. New selective lipoxygenase inhibitors

Tihanyi,Feher,Gal,et al.

, p. 433 - 439 (2007/10/02)

The synthesis and antiinflammatory activity of some new pyrazolecarboxylic acid hydrazides 3, 4 and 5 substituted with alkyl, alkylidene, aryl and acyl groups are described. 3 were prepared by reaction of pyrazolecarboxylic acids, esters, acid chlorides or diketopiperazines with hydrazines. Upon reaction with carbonyl compounds 3 gave hydrazones 4. Acylation of 3 yielded mono or bisacyl compounds 5. The most potent antiinflammatory compounds were among the N'-aryl hydrazides. These showed high lipoxygenase inhibitory activity but hardly inhibited cyclooxygenase enzyme.

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