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2,5-Cyclohexadien-1-one, 4-(4-oxo-3,5-diphenyl-2,5-cyclohexadien-1-ylidene)-2,6-diphenylis a cyclohexenone compound with a molecular structure that features a cyclohexadienone ring and four phenyl substituents. It is a yellow crystalline solid and belongs to the class of cyclohexenones.

3550-01-4

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3550-01-4 Usage

Uses

Used in Organic Synthesis:
2,5-Cyclohexadien-1-one, 4-(4-oxo-3,5-diphenyl-2,5-cyclohexadien-1-ylidene)-2,6-diphenylis used as a reagent in organic synthesis for the production of various organic compounds. Its unique molecular structure allows it to participate in a range of chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Chemical Reactions:
In the field of chemistry, 2,5-Cyclohexadien-1-one, 4-(4-oxo-3,5-diphenyl-2,5-cyclohexadien-1-ylidene)-2,6-diphenylis used as a reagent in various chemical reactions. Its ability to participate in different types of reactions, such as oxidation, reduction, and substitution, makes it a versatile compound for use in research and development.
It is important to handle 2,5-Cyclohexadien-1-one, 4-(4-oxo-3,5-diphenyl-2,5-cyclohexadien-1-ylidene)-2,6-diphenylwith care and follow appropriate safety measures when working with it in laboratory settings to ensure the safety of researchers and the integrity of the experiments.

Check Digit Verification of cas no

The CAS Registry Mumber 3550-01-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,5 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3550-01:
(6*3)+(5*5)+(4*5)+(3*0)+(2*0)+(1*1)=64
64 % 10 = 4
So 3550-01-4 is a valid CAS Registry Number.

3550-01-4SDS

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 1,5,1',5'-tetraphenyl-[3,3']bicyclohexa-1,4-dienylidene-6,6'-dione

1.2 Other means of identification

Product number -
Other names 1,5,1',5'-Tetraphenyl-[3,3']bicyclohexa-1,4-dienyliden-6,6'-dion

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:3550-01-4 SDS

3550-01-4Relevant academic research and scientific papers

Oxidative Polymerization of 2,6-Dimethylphenol to Form Poly(2,6-dimethyl-1,4-phenyleneoxide) in Water

Saito, Kei,Tago, Takahiro,Masuyama, Toru,Nishide, Hiroyuki

, p. 730 - 733 (2004)

Green polymerization: The simple stirring of 2,6-dimethylphenol with an excess of oxidant or a catalytic amount of a copper complex in an alkaline aqueous solution yields poly (2,6-dimethyl-1,4-phenyleneoxide), a commercially important polymer (see scheme). The formed polymer was easily separated as an off-white powder by filtration.

Oxidative coupling of some 2,6-disubstituted phenol derivatives in perchloric acid mediated by cerium(IV) ions

Domagala, Slawomir,Steglinska, Violetta,Dziegiec, Jozef

, p. 761 - 768 (2007/10/03)

2,6-Disubstituted phenol derivatives have been oxidized by cerium(IV) perchlorate in aqueous or aqueous-acetonitrile solutions of perchloric acid as well as in two-phase systems to the corresponding 1,4-benzoquinones, 4,4′-diphenoquinones, and oligomeric

Nitrations and Oxidations with Inorganic Nitrate Salts in Trifluoroacetic Anhydride

Crivello, J.V.

, p. 3056 - 3060 (2007/10/02)

Metal nitrates in trifluoroacetic anhydride nitrate many aromatic compounds in high yields at room temperature, including polymers with aromatic groups.However, this system oxidizes phenols to quinoid products.

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