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N-(2,2,2-trifluoro-1,1-diphenylethyl)acetamide is a complex organic compound with the molecular formula C16H14F3NO. It is a derivative of acetamide, featuring a trifluoro-diphenylethyl group attached to the nitrogen atom. This chemical is characterized by its unique structure, which includes three fluorine atoms bonded to a central carbon atom, which is also connected to two phenyl rings. The compound is known for its potential applications in various fields, such as pharmaceuticals and materials science, due to its specific properties arising from the presence of fluorine atoms and the bulky diphenylethyl group. It is important to note that the handling and use of N-(2,2,2-trifluoro-1,1-diphenylethyl)acetamide should be done with caution, as it may have specific safety and environmental considerations.

1995-76-2

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1995-76-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1995-76-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,9 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1995-76:
(6*1)+(5*9)+(4*9)+(3*5)+(2*7)+(1*6)=122
122 % 10 = 2
So 1995-76-2 is a valid CAS Registry Number.

1995-76-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2,2,2-trifluoro-1,1-diphenylethyl)acetamide

1.2 Other means of identification

Product number -
Other names Acetamide, N-(2,2,2-trifluoro-1,1-diphenylethyl)-

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:1995-76-2 SDS

1995-76-2Downstream Products

1995-76-2Relevant academic research and scientific papers

Synthesis of α-CF3 and α-CF2H amines: Via the aminofluorination of fluorinated alkenes

Yang, Ling,Fan, Wen-Xin,Lin,Tan, Dong-Hang,Li, Qingjiang,Wang, Honggen

, p. 5907 - 5910 (2018)

A novel synthesis of α-CF3 and α-CF2H amines via the aminofluorination of gem-difluoroalkenes and mono-fluoroalkenes, respectively, is reported. The method employs Selectfluor as an electrophilic fluorine source and acetonitrile as a nitrogen source. Mechanistic studies revealed a single-electron oxidation/fluorine-abstraction/Ritter-type amination pathway. The protocol allowed the synthesis of a broad range of fluorinated amines including those bearing quaternary carbon centers with good efficiency and functional group tolerance.

One Flask Preparation of Trifluoromethylated Amides from Ketones and Trifluoromethyltrimethylsilane via Ritter Reaction with Nitriles

Tongco, Emily C.,Prakash, G.K. Surya,Olah, George A.

, p. 1193 - 1195 (2007/10/03)

Trifluoromethylated amides are prepared in a simple one-flask reaction via the Ritter reaction of the corresponding trifluoromethylated silyl ethers, which themselves are readily obtained from the starting ketones and trifluoromethyltrimethylsilane. The y

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