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62635-27-2

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62635-27-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62635-27-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,6,3 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 62635-27:
(7*6)+(6*2)+(5*6)+(4*3)+(3*5)+(2*2)+(1*7)=122
122 % 10 = 2
So 62635-27-2 is a valid CAS Registry Number.

62635-27-2SDS

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 1,2-bis(2-nitrophenyl)ethane-1,2-diol

1.2 Other means of identification

Product number -
Other names 1,2-di-o-nitrophenylethylene glycol

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:62635-27-2 SDS

62635-27-2Upstream product

62635-27-2Downstream Products

62635-27-2Relevant articles and documents

Reduction of activated carbonyl groups using alkylphosphanes as reducing agents: A mechanistic study

Wei, Yin,Liu, Xu-Guang,Shi, Min

scheme or table, p. 2386 - 2393 (2012/06/04)

A comprehensive mechanistic investigation on the reduction of activated carbonyl groups using alkylphosphanes as reducing agents has been conducted through a combination of experimental as well as computational studies. Both approaches show that this kind of reduction proceeds either through proton transfer from alkylphosphanes and cleavage by water during work-up or through another reaction pathway involving the participation of water at the initial stage and a two-fold proton transfer to afford the product. The reaction mechanism of the reduction of activated carbonyl groups using alkylphosphanes has been studied both experimentally and theoretically. The reduction was shown to proceed either through proton transfer from alkylphosphanes and cleavage by water during work-up or through the participation of water at the initial stage and a two-fold proton transfer.

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