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66476-44-6

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66476-44-6 Usage

Uses

N-Methyl-N-(trifluoromethylthio)aniline is a useful research chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 66476-44-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,4,7 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 66476-44:
(7*6)+(6*6)+(5*4)+(4*7)+(3*6)+(2*4)+(1*4)=156
156 % 10 = 6
So 66476-44-6 is a valid CAS Registry Number.

66476-44-6 Well-known Company Product Price

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  • TCI America

  • (M2595)  N-Methyl-N-(trifluoromethylthio)aniline  >98.0%(GC)

  • 66476-44-6

  • 200mg

  • 790.00CNY

  • Detail
  • TCI America

  • (M2595)  N-Methyl-N-(trifluoromethylthio)aniline  >98.0%(GC)

  • 66476-44-6

  • 1g

  • 2,750.00CNY

  • Detail

66476-44-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-methyl-N-phenyl-S-(trifluoromethyl)thiohydroxylamine

1.2 Other means of identification

Product number -
Other names trifluoromethanesulfenamide

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:66476-44-6 SDS

66476-44-6Relevant articles and documents

Palladium-Catalyzed Trifluoromethylthiolation of Chelation-Assisted C–H Bonds

Kesavan, Arunachalam,Chaitanya, Manthena,Anbarasan, Pazhamalai

, p. 3276 - 3279 (2018/07/13)

An efficient palladium-catalyzed trifluoromethylthiolation of chelation-assisted C–H bonds has been accomplished by employing a readily accessible trifluoromethylthiolating reagent. The reaction tolerates various directing groups and functional groups and allows the access to diverse trifluoromethylthiolated arenes in good yield. A plausible mechanism was proposed based on preliminary mechanistic investigations.

N-Trifluoromethylthio-dibenzenesulfonimide: A Shelf-Stable, Broadly Applicable Electrophilic Trifluoromethylthiolating Reagent

Zhang, Panpan,Li, Man,Xue, Xiao-Song,Xu, Chunfa,Zhao, Qunchao,Liu, Yafei,Wang, Haoyang,Guo, Yinlong,Lu, Long,Shen, Qilong

, p. 7486 - 7509 (2016/09/09)

The super electrophilicity of a shelf-stable, easily prepared trifluoromethylthiolating reagent N-trifluoromethylthio-dibenzenesulfonimide 7 was demonstrated. Consistent with the theoretical prediction, 7 exhibits reactivity remarkably higher than that of other known electrophilic trifluoromethylthiolating reagents. In the absence of any additive, 7 reacted with a wide range of electron-rich arenes and activated heteroarenes under mild conditions. Likewise, reactions of 7 with styrene derivatives can be fine-tuned by simply changing the reaction solvents to generate trifluoromethylthiolated styrenes or oxo-trifluoromethylthio or amino-trifluoromethylthio difunctionalized compounds in high yields.

Multigram Scale Syntheses of First and Second Generation of Trifluoromethanesulfenamide Reagents

Glenadel, Quentin,Alazet, Sébastien,Baert, Fran?ois,Billard, Thierry

, p. 960 - 964 (2016/06/13)

Trifluoromethanesulfenamide reagents constitute a family of very efficient reagents to trifluoromethylthiolate various molecules. Optimized syntheses have been developed to easily obtain, in a reproducible manner, large quantities of these reagents, with good overall yields. Up to 84 g have already been obtained, at a reasonable cost.

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