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Benzamide, N-[2-[(phenylmethyl)amino]ethyl]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

67630-76-6

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67630-76-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 67630-76-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,6,3 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 67630-76:
(7*6)+(6*7)+(5*6)+(4*3)+(3*0)+(2*7)+(1*6)=146
146 % 10 = 6
So 67630-76-6 is a valid CAS Registry Number.

67630-76-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name N-[2-(benzylamino)ethyl]benzamide

1.2 Other means of identification

Product number -
Other names N-Benzyl-N'-benzoylethylendiamine

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:67630-76-6 SDS

67630-76-6Relevant academic research and scientific papers

Anion selectivity in zwitterionic amide-functionalised metal salt extractants

Galbraith, Stuart G.,Wang, Qiang,Li, Li,Blake, Alexanders,Wilson, Claire,Collinson, Simon R.,Lindoy, Leonard F.,Plieger, Paul G.,Schroeder, Martin,Tasker, Peter A.

, p. 6090 - 6107 (2008/02/13)

Amide-functionalised salen ligands capable of extracting metal salts have been synthesised and characterised. Single-crystal X-ray structure determinations of complexes of NiSO4, [Ni(L)(SO4)], confirm that the ionophores are in a zwi

Competitive amide hydrolysis in mono- and diformylated ethylenediamines

Petride, Horia,Costan, Oana,Florea, Cristina,Udrea, Silvia

, p. 245 - 253 (2007/10/03)

Alkaline hydrolysis of formylated ethylenediamines of the general structure R1-N(X)-CH2CH2-N(CHO)-R2 (R 1, R2 = H, benzyl, benzoyl; X = H, CHO) was studied in mild conditions. Breaking of the N-C amide bonds took place easily for HN-CHO or (benzoyl)N-CHO, hardly for (benzyl)N-CHO, and did not occur at all for N-COPh. Generally speaking, the various amide bonds underwent hydrolysis according to the following qualitative order of increasing reactivity: PhCO-N(H or alkyl)(alkyl or CHO) ?HCO-N(alkyl)2 1H- and 13C-NMR features of all compounds of interest are presented and discussed. Hindered rotation about the C-N amide bond(s) caused E/Z isomerism in mono- and diformylated derivatives.

Studies on development of sufficiently chemoselective N-acylation reagents: N-Acyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamides

Kondo, Kazuhiro,Sekimoto, Erika,Nakao, Junko,Murakami, Yasuoki

, p. 5843 - 5856 (2007/10/03)

A variety of storable N-acyl-N-(2,3,4,5,6-pentafluorophenyl)methanesulfonamides (4a-e) prepared from N-2,3,4,5,6-pentafluorophenylmethanesulfonamide (3), have been developed after systematic research on the structure-reactivity relationship and were found to serve as N-acylation reagents exhibiting sufficiently good chemoselectivity. (C) 2000 Elsevier Science Ltd.

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