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Ethanimidoyl chloride, N-(2,6-dimethylphenyl)-2,2,2-trifluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65158-40-9

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65158-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65158-40-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,5 and 8 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65158-40:
(7*6)+(6*5)+(5*1)+(4*5)+(3*8)+(2*4)+(1*0)=129
129 % 10 = 9
So 65158-40-9 is a valid CAS Registry Number.

65158-40-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,6-dimethylphenyl)-2,2,2-trifluoroethanimidoyl chloride

1.2 Other means of identification

Product number -
Other names N-(2,6-xylyl)-2,2,2-trifluoroacetimidoyl chloride

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:65158-40-9 SDS

65158-40-9Relevant academic research and scientific papers

2-(Trifluoromethyl)indoles via Pd(0)-Catalyzed C(sp3)-H Functionalization of Trifluoroacetimidoyl Chlorides

Pedroni, Julia,Cramer, Nicolai

supporting information, p. 1932 - 1935 (2016/06/09)

Perfluoroalkylated indoles are valuable compounds in drug discovery. A Pd(0)-catalyzed C(sp3)-H functionalization enables access to 2-(trifluoromethyl)indoles from trifluoroacetimidoyl chlorides. These are stable compounds, easily obtained from

One-Pot Synthesis of Trifluoroacetimidoyl Halides

Tamura, Kenji,Mizukami, Hiromichi,Maeda, Kazuhiro,Watanabe, Hisayuki,Uneyama, Kenji

, p. 32 - 35 (2007/10/02)

Trifluoroacetimidoyl chlorides 1 were obtained in 80-90percent yields when a mixture of trifluoroacetic acid and a primary amine was heated in carbon tetrachloride in the presence of triphenylphosphine and triethylamine.The corresponding bromides 2 were o

Homologation of trifluoroacetimidoyl iodides by palladium-catalyzed carbonylation. An approach to α-amino perfluoroalkanoic acids

Watanabe,Hashizume,Uneyama

, p. 4333 - 4336 (2007/10/02)

Homologation of trifluoroacetimidoyl iodides and the related perfluoro-compounds by palladium-catalyst under CO(1atm)-atmosphere in the presence of alcohols gives α-imino perfluoroalkanoates which are transformed to α-amino perfluoroalkanoic acids.

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