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3790-91-8

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3790-91-8 Usage

General Description

2,5-Cyclohexadiene-1,4-dione, 2-(1,1-dimethylethyl)-6-hydroxy- is a chemical compound that belongs to the class of cyclohexadiene-1,4-diones. It is a derivative of 2,5-Cyclohexadiene-1,4-dione with the hydroxy group substituted at the 6th position and a tert-butyl group at the 2nd position of the cyclohexadiene ring. 2,5-Cyclohexadiene-1,4-dione, 2-(1,1-dimethylethyl)-6-hydroxy- is used in various organic synthesis and pharmaceutical applications due to its unique structural and reactivity properties. It is known for its ability to undergo various chemical reactions, making it a valuable intermediate in the production of other organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 3790-91-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,7,9 and 0 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3790-91:
(6*3)+(5*7)+(4*9)+(3*0)+(2*9)+(1*1)=108
108 % 10 = 8
So 3790-91-8 is a valid CAS Registry Number.

3790-91-8SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 6-tert-butyl-2-hydroxy-para-benzoquinone

1.2 Other means of identification

Product number -
Other names 2-tert-Butyl-6-hydroxy-[1,4]benzochinon

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:3790-91-8 SDS

3790-91-8Relevant articles and documents

Hydroxylation of substituted diatomic phenols and their derivatives

Vol'eva,Prokof'eva,Belostotskaya,Komissarova,Ershov

, p. 1952 - 1955 (2007/10/03)

Oxidation of 3,6-di-tert-butylpyrocatechol in protic media is accompanied by the formation of 3,6-di-tert-butyl-2-hydroxy-para-benzoquinone. Hydroxylation of the 3,5-isomer results in dealkylation and isomerization with the formation of 6-tert-butyl-2-hydroxypora-benzoquinone and the quinone mentioned above, respectively. Their ratio depends on the nature of the solvent. Analogous processes accompany redox transformations of 2,6-di-tert-butylhydroquinone, 2,6-diphenyl-para-benzoquinone, and 2,4,6-tri-tert-butylphenol adsorbed on silica gel. Derivatives of 3,5-substituted pyrocatechols formed under conditions of heterophase oxidation in air are capable of transformations to form nitrogen-containing compounds.

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