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10507-25-2

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10507-25-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 10507-25-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,0 and 7 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 10507-25:
(7*1)+(6*0)+(5*5)+(4*0)+(3*7)+(2*2)+(1*5)=62
62 % 10 = 2
So 10507-25-2 is a valid CAS Registry Number.

10507-25-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name N-benzyl-N-[2-[benzyl(formyl)amino]ethyl]formamide

1.2 Other means of identification

Product number -
Other names N,N'-Dibenzyl-N,N'-diformyl-aethylendiamin

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:10507-25-2 SDS

10507-25-2Downstream Products

10507-25-2Relevant articles and documents

RuO4-mediated oxidation of N-benzylated tertiary amines. Four- And three-membered azacycloalkanes as substrates

Florea, Cristina A.,H?rtopeanu, Anca,Stavarache, Cristina,Petride, Horia

, p. 294 - 307 (2018/11/26)

Similarly to N-benzylpiperidine and -pyrrolidine, N-benzylazetidine underwent RuO4-catalyzed oxidation by attack at both types of N-methylene C-H bonds: Endocyclic and exocyclic (benzylic). If the reaction is performed in the presence of cyanide, α-aminon

Selective oxidation of piperazine derivatives with ruthenium tetroxide

Vetuschi,Tangari,Giovine,Franchini,Tortorella

, p. 599 - 605 (2007/10/02)

Diacetyl and dibenzyl piperazine were oxidized by RuO4, in order to investigate the regioselective behaviour of the reaction on piperazine substrata for the preparation of oxidized derivatives with remarkable biological activities and, in addition, as useful synthetic procedures for the identification of the metabolites of drugs. Cyclic monocarbonyl derivatives were never isolated and the two adjacent methylene groups are preferentially oxidized.

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