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3,3'-Diphenyl- is a chemical structure that refers to a specific arrangement of atoms in a molecule, where two phenyl groups (each consisting of a six-carbon ring with alternating single and double bonds, also known as benzene rings) are connected through a single bond at the 3rd carbon position on each ring. This structure is a common motif in various organic compounds and can be found in different types of molecules, such as 3,3'-diphenyl-1,1'-biphenyl, which is a symmetrical biphenyl with phenyl groups attached at the 3rd position. The 3,3'-diphenyl- structure is significant in the field of organic chemistry and material science, as it can influence the physical and chemical properties of the compounds that contain it, such as their stability, reactivity, and electronic properties.

5660-42-4

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5660-42-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5660-42-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,6,6 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 5660-42:
(6*5)+(5*6)+(4*6)+(3*0)+(2*4)+(1*2)=94
94 % 10 = 4
So 5660-42-4 is a valid CAS Registry Number.

5660-42-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3''-diphenyl-p-terphenyl

1.2 Other means of identification

Product number -
Other names 3,3''-Diphenyl-terphenyl

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:5660-42-4 SDS

5660-42-4Downstream Products

5660-42-4Relevant academic research and scientific papers

Studies of Polyphenyls and Polyphenylenes. II. The Synthesis and Physical Properties of Polyphenyls Containing Para Linkage

Ozasa, Shigeru,Hatada, Noriko,Fujioka, Yasuhiro,Ibuki, Eiichi

, p. 2610 - 2617 (2007/10/02)

Twelwe linear polyphenyls, including quinque- to octiphenyl, were synthesized by the Ullmann cross-coupling reaction of iodobiphenyl with diiodobenzene or iodoterphenyl.Ultraviolet spectral studies of the polyphenyls indicated that the positions of the K-bands above ca.260 nm, regardless of the presence of o- or m-phenylene unit(s), may be considered to be an indication of the approximate number of consecutive p-phenylene units.Infrared studies also showed that the locations of strong or medium bands in the 815-850 cm-1 region may give the same information.The HMO calculations of the longest wavelength absorption bands of twenty-four polyphenyls were carried out.A comparison between the calculated and observed wavelengths gave rather good agreement, except in the cases of two compounds.The signals of the proton magnetic resonanse spectra of eighteen polyphenyls were assigned tentatively.The correlations between the arrangement of the benzene rings and the spectral patterns are discussed.

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