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Glycine, N-benzoyl-N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

201405-92-7

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201405-92-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 201405-92-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,1,4,0 and 5 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 201405-92:
(8*2)+(7*0)+(6*1)+(5*4)+(4*0)+(3*5)+(2*9)+(1*2)=77
77 % 10 = 7
So 201405-92-7 is a valid CAS Registry Number.

201405-92-7SDS

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 2-[benzoyl(benzyl)amino]acetic acid

1.2 Other means of identification

Product number -
Other names N-Benzoyl-N-benzyl-glycin

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:201405-92-7 SDS

201405-92-7Relevant academic research and scientific papers

Electroorganic synthesis of benzathine

Lateef, Shaik,Reddy Krishna Mohan, Srinivasulu,Reddy Jayarama Reddy, Srinivasulu

, p. 77 - 80 (2007/10/03)

Benzathine is prepared in good yields from cyanobenzene by a combination of electrochemical hydrogenation and Kolbe electrolysis using nickel and platinum electrodes in the presence of methanolic sodium methoxide in an undivided cell.

Convenient synthesis of 4-trifluoromethyl-substituted imidazole derivatives

Kawase,Saito,Kurihara

, p. 461 - 464 (2007/10/03)

Mesoionic 4-trifluoroacetyl-1,3-oxazolium-5-olates (1), obtained from the reaction of N-acyl-N-alkylglycines (2) with trifluoroacetic anhydride, react with ammonia to give 4-trifluoromethyl-3,4-dihydroimidazoles (3) in high yields. Dehydration of 3 gives

The Alkylation of Menthyl Hippurate and Some Related Materials: A Reinvestigation.

McIntosh, John M.,Thangarasa, Rasiah,Foley, Nancy K.,Ager, David J.,Froen, Diane E.,Klix, Russell C.

, p. 1967 - 1974 (2007/10/02)

Benzylation of chiral esters of N-acyglycines using various bases and additives was examined.No C-alkylation was observed with one equivalent of base.Diastereoselectivities were dependent on the amount of additive, the nature of the N-acyl group, and the chiral ester.A model to account for the degree and sense of the stereoselectivity is proposed.

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