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113770-42-6

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113770-42-6 Usage

Building block

Common in organic chemistry

Unique properties

Introduction of a fluorine atom to the structure

Potential applications

Synthesis of advanced materials such as liquid crystals, polymers, and organic semiconductors

Research interest

Studying the impact of fluorine substitution on the physical and chemical properties of organic compounds

Scientific community

Garnered interest for various research and industrial applications

Check Digit Verification of cas no

The CAS Registry Mumber 113770-42-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,3,7,7 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 113770-42:
(8*1)+(7*1)+(6*3)+(5*7)+(4*7)+(3*0)+(2*4)+(1*2)=106
106 % 10 = 6
So 113770-42-6 is a valid CAS Registry Number.

113770-42-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-fluoro-1,4-diphenylbenzene

1.2 Other means of identification

Product number -
Other names 1,1':4',1''-Terphenyl,2'-fluoro

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:113770-42-6 SDS

113770-42-6Relevant articles and documents

Electrosynthesis of functionalized organodizinc compounds from aromatic dihalides via a cobalt catalysis in acetonitrile/pyridine as solvent

Fillon, Hyacinthe,Gosmini, Corinne,Nédélec, Jean-Yves,Périchon, Jacques

, p. 3843 - 3846 (2007/10/03)

Electroreduction of aryl-dichlorides or -dibromides in an electrochemical cell fitted with a sacrificial zinc anode and in the presence of cobalt halides as catalyst in acetonitrile/pyridine as solvent affords the corresponding organodizinc species in moderate to excellent yields with high selectivity.

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