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Diazene, bis(2-chloro-2-methylcyclohexyl)-, 1,2-dioxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

88934-90-1

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88934-90-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 88934-90-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,3 and 4 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 88934-90:
(7*8)+(6*8)+(5*9)+(4*3)+(3*4)+(2*9)+(1*0)=191
191 % 10 = 1
So 88934-90-1 is a valid CAS Registry Number.

88934-90-1SDS

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-chloro-2-methylcyclohexyl)-[(2-chloro-2-methylcyclohexyl)-oxidoamino]-oxoazanium

1.2 Other means of identification

Product number -
Other names Diazene,bis(2-chloro-2-methylcyclohexyl)-,1,2-dioxide

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:88934-90-1 SDS

88934-90-1Upstream product

88934-90-1Relevant academic research and scientific papers

Specific Inhibitors in Vitamin Biosynthesis. Part 7. Syntheses of Blocked 7,8-Dihydropteridines via &α-Amino Ketones

Al-Hassan, Saiba S.,Cameron, Robert J.,Curran, Adrian W. C.,Lyall, William J. S.,Nicholson, Sydney H.,et al.

, p. 1645 - 1660 (2007/10/02)

The synthesis of 15 blocked 7,8-dihydropteridines is described in which the pyrazine ring is built from a derivative of an α-amino ketone.Three routes to the amino ketones based upon amino acids, nitrosyl chloride addition to alkenes, and nitro alcohols are discussed.The compounds synthesised are inhibitors of 6-hydroxymethyl-7,8-dihydropterin pyrophosphokinase , an enzyme in the pathway leading to dihydrofolate, and the inhibitory potencies of the compounds are discussed in the light of a hypothetical active site model for the enzyme.

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