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3,5-Cyclohexadiene-1,2-dione, 3-(1,1-dimethylethyl)-6-methyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

62870-14-8

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62870-14-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 62870-14-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,8,7 and 0 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62870-14:
(7*6)+(6*2)+(5*8)+(4*7)+(3*0)+(2*1)+(1*4)=128
128 % 10 = 8
So 62870-14-8 is a valid CAS Registry Number.

62870-14-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-tert-butyl-6-methylcyclohexa-3,5-diene-1,2-dione

1.2 Other means of identification

Product number -
Other names 3-tert-butyl-6-methyl-1,2-benzoquinone

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:62870-14-8 SDS

62870-14-8Relevant academic research and scientific papers

Study of the reaction of 3,6-di-tert-butyl-o-benzoquinone with organozinc and organocadmium compounds

Kurskii, Yu. A.,Druzhkov,Egorochkin,Abakumov

, p. 37 - 42 (2016)

The effect of substituents in the reactions of 3,6-di-tert-butyl-o-benzoquinone with organozinc and organocadmium compounds, leading to three types of products: 3-alkyl-6-tert-butyl-o-benzoquinones, 4-alkyl-3,6-di-tert-butyl-o-benzoquinones, and 2-alkoxy-(or 2-phenoxy)-3,6-di-tert-butylphenols. Correlation analysis gave evidence to show that the first- and second-type products are formed by nucleophilic 1,2- and 1,4-addition, while substituted phenols result from single-electron transfer.

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