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1H-Pyrazole-1-carbothioamide, 4,5-dihydro-3-methyl-5-oxo-4-(phenylhydrazono)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

26178-92-7

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26178-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 26178-92-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,1,7 and 8 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26178-92:
(7*2)+(6*6)+(5*1)+(4*7)+(3*8)+(2*9)+(1*2)=127
127 % 10 = 7
So 26178-92-7 is a valid CAS Registry Number.

26178-92-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-thiocarboxamido-3-methyl-4-(phenylhydrazono)-2-pyrazolin-5-one

1.2 Other means of identification

Product number -
Other names 4-phenylhydrazono-N'-thiocarbamoyl-3-methyl-2-pyrazolin-5-one

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:26178-92-7 SDS

26178-92-7Relevant academic research and scientific papers

Sydnone derivatives. Part VII: Synthesis of some novel thiazoles and their pharmacological properties

Kalluraya, Balakrishna,Rahiman, M. Abdul,Banji, David

, p. 263 - 268 (2007/10/03)

The synthesis of some 4-(arylsydnonyl)-2- (4-arylhydrazono-3-methyl-5-oxo-2-pyrazolin-1-yl)-thiazoles by reacting 1-thiocarboxamido-3-methyl-4-(arylhydrazono)-2-pyrazolin-5-ones with different 4-bromoacetyl-3-arylsydnones is described. A few compounds from this series were screened for their anti-inflammatory, analgesic, and CNS depressant activities. Among the tested compounds 6s, 6d, 6n, and 6u showed significant anti-inflammatory activity comparable with that of standard drug Ibuprofen. Compounds containing chlorine and carboxylic substituents are more active. 6f, 6r, and 6u showed marked analgesic activity and most of the compounds tested showed promising CNS depressant activity comparable with that of standard drug pentobarbitone.

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