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Carbonyldibenzene-4,1-diyl diacetate, also known as 1,4-diacetoxybenzene, is an organic compound with the chemical formula C10H8O4. It is a colorless crystalline solid that is soluble in organic solvents. carbonyldibenzene-4,1-diyl diacetate is formed by the acetylation of 1,4-benzenediol (hydroquinone), where two acetate groups are attached to the hydroxyl groups of the benzene ring. Carbonyldibenzene-4,1-diyl diacetate is used as an intermediate in the synthesis of various chemical compounds, particularly in the production of pharmaceuticals and dyes. It is also known for its potential applications in the preparation of polymers and as a reagent in organic synthesis. The compound is characterized by its stability and reactivity, which makes it a valuable building block in the chemical industry.

6290-82-0

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6290-82-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6290-82-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,2,9 and 0 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 6290-82:
(6*6)+(5*2)+(4*9)+(3*0)+(2*8)+(1*2)=100
100 % 10 = 0
So 6290-82-0 is a valid CAS Registry Number.

6290-82-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name [4-(4-acetyloxybenzoyl)phenyl] acetate

1.2 Other means of identification

Product number -
Other names 4,4'-diacetoxy-benzophenone

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:6290-82-0 SDS

6290-82-0Relevant academic research and scientific papers

Electrochemical Aerobic Oxidative Cleavage of (sp3)C-C(sp3)/H Bonds in Alkylarenes

Liu, Shuai,Liu, Zhong-Quan,Shen, Tong,Shen, Xu,Wang, Nengyong,Wu, Jintao,Yang, Le,Zhao, Jianyou

, p. 3286 - 3295 (2022/03/14)

An electrochemistry-promoted oxidative cleavage of (sp3)C-C(sp3)/H bonds in alkylarenes was developed. Various aryl alkanes can be smoothly converted into ketones/aldehydes under aerobic conditions using a user-friendly undivided cell setup. The features of air as oxidant, scalability, and mild conditions make them attractive in synthetic organic chemistry.

Phosphine ligand triggered oxidative decarbonylative homocoupling of aromatic aldehydes: Selectively generating biaryls and diarylketones

Yang, Luo,Zeng, Tieqiang,Shuai, Qi,Guo, Xiangyu,Li, Chao-Jun

supporting information; experimental part, p. 2161 - 2163 (2011/03/22)

A novel rhodium-catalyzed oxidative decarbonylative homocoupling of aromatic aldehydes to generate biaryls and diarylketones selectively and efficiently, triggered by the choice of different phosphine ligands.

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