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N-tert-butyl-2-chloro-2-phenylacetamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

65117-34-2

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65117-34-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 65117-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,1,1 and 7 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65117-34:
(7*6)+(6*5)+(5*1)+(4*1)+(3*7)+(2*3)+(1*4)=112
112 % 10 = 2
So 65117-34-2 is a valid CAS Registry Number.

65117-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name N-tert-butyl-2-chloro-2-phenylacetamide

1.2 Other means of identification

Product number -
Other names N-tert-butyl-2-chloro-2-phenylethanamide

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:65117-34-2 SDS

65117-34-2Relevant academic research and scientific papers

Base-Promoted Reaction of O-Sulfonylated Hydroxamic Acids with Nucleophiles. A New Mehtod for the Synthesis of α-Substituted Amides

Hoffman, Ribert V.,Nayyar, Naresh K.,Chen, Wenting

, p. 5700 - 5707 (2007/10/02)

Treatment of a series of hydroxamic acids 2 with mesyl chloride in the presence of 2 equiv of triethylamine at 0 deg C gives 2-chloroamides 3 in good yields.Use of a single equivalent of triethylamine gives the N-(mesyloxy)amides 1, which are versatile sy

4-Imidazolidinones from Nitrones and Isocyanides. - Molecular Structure of 5-tert-Butyl-1,2,2-trimethyl-3-(2,4,6-tribromophenyl)-4-imidazolidinone

Moderhack, Dietrich,Lorke, Michael,Schomburg, Dietmar

, p. 1685 - 1695 (2007/10/02)

Certain reactions of nitrone 1 and isocyanide 2, in the presence of ether-boron trifluoride, afford 4-imidazolidinones 4 which have been shown to be ring expansion products of the 4-imino-1,2-oxazetidines 3. 1,2,4-Oxadiazolidin-5-ones 5 (rather than 3 or

The Thermal Decomposition of N,O-Diacyl-N-t-butylhydroxylamines. IV. A Novel Acyloxyl Migration in N,O-Diacyl-N-t-butylhydroxylamines

Uchida, Yuzuru,Kozuka, Seizi

, p. 2681 - 2682 (2007/10/02)

Several N,O-diacyl-N-t-butylhydroxylamines were prepared, and their thermal decompositions were studied.N-Propionyl-O-benzoyl-N-t-butylhydroxylamine gave N-t-butyl-2-benzoyloxypropanamide, together with the decomposition products, N-t-butylpropanamide and benzoic acid, upon thermal decomposition in tetralin.Similar benzyloxyl migrations were found in the thermal decomposition of N-butyryl, N-valeryl, and N-(3-phenylpropionyl) derivatives.

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