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2-phenyl-5-[4-(5-phenyl-2-thienyl)phenyl]thiophene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

256342-39-9

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256342-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 256342-39-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,6,3,4 and 2 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 256342-39:
(8*2)+(7*5)+(6*6)+(5*3)+(4*4)+(3*2)+(2*3)+(1*9)=139
139 % 10 = 9
So 256342-39-9 is a valid CAS Registry Number.

256342-39-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-phenyl-5-[4-(5-phenylthiophen-2-yl)phenyl]thiophene

1.2 Other means of identification

Product number -
Other names Thiophene,2,2'-(1,4-phenylene)bis[5-phenyl

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:256342-39-9 SDS

256342-39-9Downstream Products

256342-39-9Relevant academic research and scientific papers

Synthesis of thiophene/phenylene co-oligomers. II [1]. Block and alternating co-oligomers

Hotta,Kimura,Lee,Tamaki

, p. 281 - 286 (2007/10/03)

We report the synthesis of block and alternating thiophene/phenylene co- oligomers that is based either on the Suzuki coupling reaction or on the Grignard reaction. These reaction schemes enable us to obtain the target compounds at reasonably high yields.

The preparations and some properties of mixed aryl-thienyl oligomers and polymers

Pelter, Andrew,Jenkins, Ieuan,Jones, D. Elfyn

, p. 10357 - 10400 (2007/10/03)

The syntheses by transition metal coupling reactions of a large number of oligomers constructed from benzene and thiophene rings are described. The first use of arylcadmium chlorides for such coupling reactions is reported. The routes chosen allow for rational variation in the modes of linkage, the substitution and the proportions of the two units. The benzene and thiophene rings are always joined in a known order and may bear a wide variety of regularly spaced functional groups. Additionally the shape of the oligomers may be varied at will. In all cases p-type doping with iodine or ferric chloride leads to large enhancements in conductivity.

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