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2,6-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

78102-66-6

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78102-66-6 Usage

Isomer

2,6-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one is an isomer of another compound with the same molecular formula, meaning they have the same number and type of atoms but arranged differently.

Highly reactive

Due to its structure, 2,6-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one readily undergoes chemical reactions, making it useful in the synthesis of various organic compounds.

Precursor in pharmaceuticals and agrochemicals

It serves as a starting material or building block for the production of various pharmaceutical and agrochemical products.

Antioxidant properties

It helps prevent the oxidation of other substances, making it a valuable component in the food and cosmetic industries to maintain product quality and stability.

Biological activities

The compound has been studied for its potential therapeutic effects, such as anti-inflammatory and anticancer properties.

Check Digit Verification of cas no

The CAS Registry Mumber 78102-66-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,8,1,0 and 2 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 78102-66:
(7*7)+(6*8)+(5*1)+(4*0)+(3*2)+(2*6)+(1*6)=126
126 % 10 = 6
So 78102-66-6 is a valid CAS Registry Number.

78102-66-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,6-dihydroxy-4,4-dimethylcyclohexa-2,5-dien-1-one

1.2 Other means of identification

Product number -
Other names 2,6-dihydroxy-4,4-dimethyl-2,5-cyclohexadien-1-one

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:78102-66-6 SDS

78102-66-6Relevant academic research and scientific papers

THE FLUORIDE ION EFFECT IN THE REACTIONS OF SINGLET OXYGEN WITH ENOLS

Wasserman, Harry H.,Pickett, James E.

, p. 2155 - 2162 (2007/10/02)

The fluoride ion effect in the reaction of enolic systems with singlet oxygen has been investigated. β-Dicarbonyl compounds yielded 1,2,3-tricarbonyl derivatives, some of which underwent further hydration, whereas α-diketones suffered oxidative decarboxylation to give open-chain aldehydo-acids or keto-acids.

1,2,3-Cyclohexanetrione/2,6-Dihydroxy-2,5-cyclohexadien-1-one Isomerization: A Facile Synthesis of 2,6-Dioxy-substituted 2,5-Cyclohexadien-1-ones

Schank, Kurt,Blattner, Rudolf,Bouillon, Guenter

, p. 1951 - 1957 (2007/10/02)

Hitherto unknown 1,2,3-cyclohexanetriones 5 masked as chlorohydrins 2 or as chlorohydrin esters 4 are easily rearranged yielding the corresponding 2,6-dihydroxy-2,5-cyclohexadien-1-ones 6 or their ester 8.

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