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62351-54-6

62351-54-6

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62351-54-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62351-54-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,3,5 and 1 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62351-54:
(7*6)+(6*2)+(5*3)+(4*5)+(3*1)+(2*5)+(1*4)=106
106 % 10 = 6
So 62351-54-6 is a valid CAS Registry Number.

62351-54-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-N-(2,2,2-trifluoroethyl)aniline

1.2 Other means of identification

Product number -
Other names o-Tolyl-(2,2,2-trifluoro-ethyl)-amine

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:62351-54-6 SDS

62351-54-6Downstream Products

62351-54-6Relevant articles and documents

Iron porphyrin-catalyzedN-trifluoroethylation of anilines with 2,2,2-trifluoroethylamine hydrochloride in aqueous solution

Guo, Cancheng,Guo, Yongjia,Liu, Qiang,Ren, Shuang,Xu, Guiming

, p. 20322 - 20325 (2021/06/26)

An iron porphyrin-catalyzedN-trifluoroethylation of anilines has been developed with 2,2,2-trifluoroethylamine hydrochloride as the fluorine source. This one-pot N-H insertion reaction is conductedviacascade diazotization/N-trifluoroethylation reactions.

PALLADIUM-CATALYZED ARYLATION OF FLUOROALKYLAMINES

-

Paragraph 0067; 0079, (2016/12/01)

Methods for synthesizing trifluoroethyl, difluoroethyl, pentafluoropropyl, and difluorophenethyl anilines by palladium-catalyzed coupling of fluoroalkylamines with aryl bromides and aryl chlorides are provided herein. The reaction is conducted with a weak

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