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81303-58-4

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81303-58-4 Usage

Derivative of pyrazole

yes

Contains a carbonyl chloride group

yes

Contains a cyano group

yes

Commonly used in organic synthesis

yes

Used in production of pharmaceuticals and agrochemicals

yes

Versatile building block for synthesis of biologically active molecules

yes

Reactive carbonyl chloride and cyano functional groups

yes

Wide range of applications in the chemical industry

yes

Valuable reagent for development of new compounds with potential medicinal and agricultural uses

yes

Check Digit Verification of cas no

The CAS Registry Mumber 81303-58-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,3,0 and 3 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81303-58:
(7*8)+(6*1)+(5*3)+(4*0)+(3*3)+(2*5)+(1*8)=104
104 % 10 = 4
So 81303-58-4 is a valid CAS Registry Number.

81303-58-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-cyano-1-methylpyrazole-4-carbonyl chloride

1.2 Other means of identification

Product number -
Other names 1H-PYRAZOLE-4-CARBONYL CHLORIDE,3-CYANO-1-METHYL

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:81303-58-4 SDS

81303-58-4Downstream Products

81303-58-4Relevant articles and documents

Development of Cyanopyrazoles as Building Blocks to Fungicide Fluxapyroxad and Analogues

Zhang, Yue,Chen, Zhen,Nie, Jing,Zhang, Fa-Guang,Ma, Jun-An

, p. 7148 - 7158 (2019/06/14)

Herein, we present a facile approach to a diverse collection of 1,4-disubstituted 3-di- or mono-fluoromethylpyrazoles utilizing our previously developed cyanopyrazoles as key building blocks. This method features several merits, such as easily accessible starting materials, broad substrate scope, mild reaction conditions, and simple operation. This protocol further deserves to be highlighted by the successful translation into the synthesis of commercialized fungicide fluxapyroxad and its analogues.

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