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Ethanone, 1-[5-(1,1-dimethylethyl)-2,3-dihydroxyphenyl]- (9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

84296-64-0

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84296-64-0 Usage

Preparation

Obtained by irradiation of a benzene solution of 4-tert-butyl-o-benzoquinone in the presence of a large excess of acetaldehyde (20%).

Check Digit Verification of cas no

The CAS Registry Mumber 84296-64-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,2,9 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 84296-64:
(7*8)+(6*4)+(5*2)+(4*9)+(3*6)+(2*6)+(1*4)=160
160 % 10 = 0
So 84296-64-0 is a valid CAS Registry Number.

84296-64-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-(5-tert-Butyl-2,3-dihydroxy-phenyl)-ethanone

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:84296-64-0 SDS

84296-64-0Downstream Products

84296-64-0Relevant academic research and scientific papers

The Formation of Acetylcatechol in the Photochemical Reaction of o-Benzoquinones with Acetaldehyde

Takuwa, Akio,Iwamoto, Hidetoshi,Soga, Osamu,Maruyama, Kazuhiro

, p. 3657 - 3658 (1982)

The irradiation of several alkyl-substituted o-benzoquinones in the presence of acetaldehyde gave the corresponding acetylcatechol and catechol monoacetates via the attack of the acetyl radical on the ground-state quinone molecule.In the reaction of 3,5-di-t-butyl- and 3-t-butyl-5-methyl-o-benzoquinones, the dimer of alkyl-substituted cyclopentadienone, generated by the photodecarbonylation of the quinones, was also obtained.

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