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Benzamide, N,N'-1,2-ethanediylbis[N-(phenylmethyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

82126-37-2

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82126-37-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 82126-37-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,2,1,2 and 6 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 82126-37:
(7*8)+(6*2)+(5*1)+(4*2)+(3*6)+(2*3)+(1*7)=112
112 % 10 = 2
So 82126-37-2 is a valid CAS Registry Number.

82126-37-2SDS

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-[benzoyl(benzyl)amino]ethyl]-N-benzylbenzamide

1.2 Other means of identification

Product number -
Other names N,N'-dibenzoyl-N,N'-dibenzylethylenediamine

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:82126-37-2 SDS

82126-37-2Downstream Products

82126-37-2Relevant 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.

SYNTHESIS WITH SILICON DERIVATIVES: NON SYMMETRICAL DERIVATIZATION OF SYMMETRICAL DIAMINES

Schwartz, Eduard,Shanzer, Abraham

, p. 979 - 982 (2007/10/02)

The conversion of symmetrical diamines to monoamides via the use of cyclic siliconnitrogen compounds as intermediates is described.

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