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1H-Pyrazole-3,4-dicarboxylic acid, 1-(4-chlorophenyl)-5-methyl-, dimethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

92126-19-7

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92126-19-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92126-19-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,1,2 and 6 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 92126-19:
(7*9)+(6*2)+(5*1)+(4*2)+(3*6)+(2*1)+(1*9)=117
117 % 10 = 7
So 92126-19-7 is a valid CAS Registry Number.

92126-19-7SDS

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 dimethyl 1-(4-chlorophenyl)-5-methyl-1H-pyrazole-3,4-dicarboxylate

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:92126-19-7 SDS

92126-19-7Relevant academic research and scientific papers

Rhodium-catalyzed addition-cyclization of hydrazines with alkynes: Pyrazole synthesis via unexpected C-N bond cleavage

Li, Deng Yuan,Mao, Xiao Feng,Chen, Hao Jie,Chen, Guo Rong,Liu, Pei Nian

supporting information, p. 3476 - 3479 (2014/07/21)

Rhodium-catalyzed addition-cyclization of hydrazines with alkynes has been achieved to afford highly substituted pyrazoles under mild conditions. The cascade reaction involves two transformations: addition of the C-N bond of hydrazines to alkynes via unex

Synthesis and evaluation of furan, thiophene, and azole bis[(carbamoyloxy)methyl] derivatives as potential antineoplastic agents

Anderson,Jones

, p. 1559 - 1565 (2007/10/02)

A series of bis(hydroxymethyl)-substituted heterocycles were synthesized and converted to the corresponding bis(methylcarbamate) derivatives. The heterocyclic systems studied were based on 2-phenyl-3-methylfuran, 1-phenylpyrazole, 1-phenyl-5-methylpyrazole, 1-phenyl-5-methylthiopene, 1-phenyl-1,2,3-triazole, 3-phenylisoxazole, 3-phenylisothiazole, 2-phenylthiazole, and 2-phenyloxazole. None of the bis(carbamates) prepared was active against murine P388 lymphocytic leukemia. Pyrrole bis(carbamate), which exhibited antileukemic activity, also showed reactivity toward 4-(p-nitrobenzyl)pyridine while the inactive bis(carbamates) were unreactive in the 4-(p-nitrobenzyl)pyridine assay.

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