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1004096-15-4

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1004096-15-4 Usage

Chemical structure

Pyrazole derivative with a difluoromethyl and a methyl group attached to the pyrazole ring

Potential applications

a. Pharmaceuticals
b. Agrochemicals

Use

Building block in the synthesis of novel compounds for various purposes

Presence of fluorine atoms

Enhances potential as a bioactive molecule

Biological activities

May exhibit interesting biological activities for further research and development in the chemical industry

Check Digit Verification of cas no

The CAS Registry Mumber 1004096-15-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,0,4,0,9 and 6 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1004096-15:
(9*1)+(8*0)+(7*0)+(6*4)+(5*0)+(4*9)+(3*6)+(2*1)+(1*5)=94
94 % 10 = 4
So 1004096-15-4 is a valid CAS Registry Number.

1004096-15-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(Difluoromethyl)-5-methyl-1H-pyrazole

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:1004096-15-4 SDS

1004096-15-4Downstream Products

1004096-15-4Relevant articles and documents

N-Difluoromethylation of monosubstituted polydentate azoles

Petko, Kirill I.,Sokolenko, Taras M.,Filatov, Andrey A.,Polovinko, Vitaliy V.,Rusanov, Eduard B.,Dudko, Vadim A.,Yagupolskii, Yurii L.

, p. 359 - 366 (2019)

[Figure not available: see fulltext.] This study was focused on N-difluoromethylation of monosubstituted polydentate azoles (imidazoles, pyrazoles, and 1,2,4-triazoles) having two or three reactive sites. The substituent effects and role of reaction conditions in determining the product ratio was explored. In the majority of cases, the obtained mixtures of isomers were separated. The target products containing halogen substituents, amino or carboxy groups in the ring can serve as valuable starting compounds in the synthesis of practically useful products.

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