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83575-18-2

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83575-18-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83575-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,5,7 and 5 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 83575-18:
(7*8)+(6*3)+(5*5)+(4*7)+(3*5)+(2*1)+(1*8)=152
152 % 10 = 2
So 83575-18-2 is a valid CAS Registry Number.

83575-18-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-dicyanocyclohexa-1,3-diene-1,4-diol

1.2 Other means of identification

Product number -
Other names -

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:83575-18-2 SDS

83575-18-2Relevant articles and documents

THE HYDROCYANATION OF FREE AND POLYMER-BOUND BENZOQUINONE

Perry, Gregory J.,Sutherland, Maurice D.

, p. 1471 - 1476 (2007/10/02)

The polimer-bound quinone 2 has been prepared and used in column form with organic solvents for the convenient preparation of other quinones.In contrast to the solution reaction hydrocyanation of this quinone by the Thiele-Meisenheimer reaction did not yield a useful proportion of polymer-bound dicyanohydroquinone but instead gave a mixture of products including much monocyanohydroquinone.Helferich and Bodenbender's 2,3-dicyanocyclohexan-1,4-dione is in fact wholly the di-enol and is a likely intermediate in the hydrocyanation of benzoquinone, being oxidised by the latter to 2,3-dicyanocyclohex-2-ene-1,4-dione which tautomerises to the observed product, 2,3-dicyanohydroquinone.A lower accessibility to polymer-bound reactants as compared with those in solution is implied by these results.

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