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5-cyano-N-methyl-1-(1-methylcyclopentyl)-1H-pyrazole-4-carboxamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

119741-56-9

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119741-56-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 119741-56-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,9,7,4 and 1 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 119741-56:
(8*1)+(7*1)+(6*9)+(5*7)+(4*4)+(3*1)+(2*5)+(1*6)=139
139 % 10 = 9
So 119741-56-9 is a valid CAS Registry Number.

119741-56-9SDS

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 5-cyano-N-methyl-1-(1-methylcyclopentyl)-1H-pyrazole-4-carboxamide

1.2 Other means of identification

Product number -
Other names 5-cyano-1-(1-methylcyclopentyl)-N-methyl-1H-pyrazole-4-carboxamide

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:119741-56-9 SDS

119741-56-9Downstream Products

119741-56-9Relevant academic research and scientific papers

Alkylation of 3(5)-cyano-1H-pyrazole-4-carboxylic acid esters

-

, (2008/06/13)

The present invention provides a process for selectively alkylating pyrazoles comprising reacting a 3(5)-cyano-1H-pyrazole-4-carboxylic acid ester with a C4 -C8 alkene, or a C5 -C6 cycloalkene substituted at the 1-position with a C1 -C4 alkyl group, and a strong acid in a solvent which contains a strong electron withdrawing group. Also provided are new 3(5)-cyano-1H-pyrazole-4-carboxylic acid ester useful as starting materials in the process of the invention.

Alkylation Studies with 5-Cyano-1H-pyrazole-4-carboxylic Acid, Ethyl Ester

Beck, James R.,Aikins, James,Lynch, Michael P.,Rizzo, John R.,Tao, Eddie V.P.

, p. 3 - 6 (2007/10/02)

5-Cyano-1H-pyrazole-4-carboxylic acid, ethyl ester (1) was regioselectively alkylated at N-1 by tertiary carbocations utilizing sulfuric acid catalysis and relatively mild conditions.In the presence of boron trifluoride, the alkylation occured regioselectively at N-2.Reaction of 1 with alkyl halides under basic conditions resulted in mixture of the two isomers with alkylation at N-2 predominating.

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