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Ethanone, 1,1'-(1,4-phenylene)bis[2-phenyl-, also known as bis(2-phenyl-2-oxoethyl)benzene, is an organic compound with the chemical formula C20H16O2. It is a white crystalline solid that is soluble in organic solvents. Ethanone, 1,1'-(1,4-phenylene)bis[2-phenyl- is characterized by its symmetrical structure, featuring two phenyl-ethanone (acetophenone) groups connected by a 1,4-phenylene bridge. It is used in the synthesis of various organic compounds and as a chemical intermediate in the pharmaceutical and chemical industries. The compound is also known for its potential applications in materials science, such as in the development of novel polymers and as a precursor in the synthesis of complex organic molecules.

3363-92-6

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3363-92-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3363-92-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,6 and 3 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3363-92:
(6*3)+(5*3)+(4*6)+(3*3)+(2*9)+(1*2)=86
86 % 10 = 6
So 3363-92-6 is a valid CAS Registry Number.

3363-92-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-1-[4-(2-phenylacetyl)phenyl]ethanone

1.2 Other means of identification

Product number -
Other names 1,4-Diphenacetyl-benzol

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:3363-92-6 SDS

3363-92-6Relevant academic research and scientific papers

SYNTHESIS WITH α-HETEROSUBSTITUTED PHOSPHONATE CARBANIONS. XVII. PREPARATION OF DIACYLATED AROMATICS

Zimmer, Hans,Servay, Thomas K.

, p. 201 - 204 (2007/10/02)

Dianions derived from tetraphenyl arylene-bis--bis-phsphonates react with aromatic and heteroaromatic aldehydes to yield bis-acylated aromatics. Key words: α-Heterosubstituted phosphonate carbanions; diacylated heteroaromatics;

METHODS FOR SYNTHESIS OF AROMATIC BIS-1,2-DIKETONES, BISMETHOXYSTYRYLS, AND BISDEOXYBENZOINS FROM 1,4-DISTYRYLBENZENE

Filimonov, V. D.,Yusubov, M. S.,Ogorodnikov, V. D.

, p. 753 - 756 (2007/10/02)

trans,trans-1,4-Distyrylbenzene was converted finally into 1,4-di(phenylglyoxaloyl)benzene by methoxybromination of the double bonds with N-bromosuccinimide in methanol, dehydrobromination, hydrolysis, and oxidation of the intermediate products.The methoxybromination is stereoselective but not regioselective.

Preparation of diketones

-

, (2008/06/13)

A method for preparing diketone starting materials useful in synthesizing tetraketone precursors for high temperature resistant polyquinoxaline resins. Dicarboxylic acid derivatives that contain no alpha hydrogens are contacted in the presence of a strong

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