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3-Methyl-4-(trifluoroMethyl)-1H-pyrazole 3-Methyl-4-trifluoroMethylpyrazole is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

864239-61-2

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864239-61-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 864239-61-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,2,3 and 9 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 864239-61:
(8*8)+(7*6)+(6*4)+(5*2)+(4*3)+(3*9)+(2*6)+(1*1)=192
192 % 10 = 2
So 864239-61-2 is a valid CAS Registry Number.

864239-61-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-methyl-4-(trifluoromethyl)-1H-pyrazole

1.2 Other means of identification

Product number -
Other names 3-methyl-4-trifluoromethylpyrazole

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:864239-61-2 SDS

864239-61-2Downstream Products

864239-61-2Relevant academic research and scientific papers

Trifluoromethylation of various aromatic compounds by CF3I in the presence of Fe(II) compound, H2O2 and dimethylsulfoxide

Kino, Tatsuhito,Nagase, Yu,Ohtsuka, Yuhki,Yamamoto, Kyoko,Uraguchi, Daisuke,Tokuhisa, Kenji,Yamakawa, Tetsu

, p. 98 - 105 (2010)

Trifluoromethylation of aromatic and hetero-aromatic compounds by CF3I in the presence of Fe(II) compound, H2O2 and dimethylsulfoxide was investigated. Various trifluoromethylated benzene derivatives, six-membered nitrogen-containing aromatic compounds and five-membered hetero-aromatic compounds were obtained under mild conditions. General orientation of electrophilic substitution of aromatic compounds was observed similarly as reported in other radical trifluoromethylation previously.

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