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1,1':3',1'':3'',1''':4''',1'''':3'''',1'''''-Sexiphenyl(6CI,7CI,8CI,9CI) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

15039-46-0

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15039-46-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 15039-46-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,0,3 and 9 respectively; the second part has 2 digits, 4 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 15039-46:
(7*1)+(6*5)+(5*0)+(4*3)+(3*9)+(2*4)+(1*6)=90
90 % 10 = 0
So 15039-46-0 is a valid CAS Registry Number.

15039-46-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-phenyl-3-[3-[4-(3-phenylphenyl)phenyl]phenyl]benzene

1.2 Other means of identification

Product number -
Other names 3,4'-Di-biphenyl-3-yl-biphenyl

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:15039-46-0 SDS

15039-46-0Downstream Products

15039-46-0Relevant academic research and scientific papers

Syntheses and Spectral Properties of Several Unsymmetrical Sexiphenyls

Ozasa, Shigeru,Fujioka, Yasuhiro,Ibuki, Eiichi

, p. 2698 - 2704 (2007/10/02)

Six sexiphenyls, including four new isomers, 2,3'-di(4-biphenylyl)biphenyl (2), 4-(2-biphenylyl)-o- (4), 4-(2-biphenylyl)-m-quaterphenyl (5), and 2-phenyl-p-quinquephenyl (6), were synthesized by the Ullmann cross-coupling of iodobiphenyl and diiodobiphenyl or of two kinds of iodoterphenyls.The characteristic bands of the infrared spectra (680-920 cm-1) and signals of the proton magnetic resonance spectra of the sexiphenyls were assigned tentatively and are discussed briefly.The remarkable high field shifts of the p-phenylene proton signals in 4 (1.23 and 0.89 ppm) as compared with that of p-terphenyl (δ 7.68) presumably reflect the ring current effects caused by the presence of adjacent o-phenylene rings.Ultraviolet spectral studies indicated that the absorption curves of the sexiphenyls were related closely to those of the polyphenyls corresponding to their partial structures.Keywords-Ullmann reaction; IR; UV; 1H-NMR; sexiphenyls; polyphenyls

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