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2,2'-Bithiophene, 5-butyl- is an organic compound with the chemical formula C12H12S2. It is a derivative of bithiophene, a heterocyclic compound consisting of two thiophene rings fused together. The butyl group is attached to the 5-position of the bithiophene backbone, which influences its chemical and physical properties. 2,2'-Bithiophene, 5-butyl- is primarily used in the synthesis of various organic materials, such as polymers and oligomers, and has potential applications in the field of organic electronics, including organic solar cells and organic light-emitting diodes (OLEDs). Its unique structure and properties make it an interesting candidate for further research and development in the area of advanced materials.

3216-81-7

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3216-81-7 Usage

Structure

Two thiophene rings attached at the 2 and 2' positions, with a butyl group attached to the 5th position of one of the rings

Usage

Organic electronics and materials science

Electronic properties

High-performance organic semiconductor

Potential applications

+ Organic light-emitting diodes (OLEDs)
+ Organic photovoltaics (OPVs)
+ Organic field-effect transistors (OFETs)

Synthesis

Can be used as a building block in the synthesis of more complex organic materials and compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 3216-81-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,1 and 6 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 3216-81:
(6*3)+(5*2)+(4*1)+(3*6)+(2*8)+(1*1)=67
67 % 10 = 7
So 3216-81-7 is a valid CAS Registry Number.

3216-81-7SDS

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 5-butyl-2,2'-bithiophene

1.2 Other means of identification

Product number -
Other names -

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:3216-81-7 SDS

3216-81-7Downstream Products

3216-81-7Relevant academic research and scientific papers

Alkylated 2,2′-bithiophenes and 2-phenylthiophenes in the composition of pyrolysis products of high-sulfur kerogen

Bushnev

, p. 184 - 192 (2007)

Compounds from the 5-n-alkyl-2,2′-bithiophene, 5-n-alkyl-5′- methyl-2,2′-bithiophene, 5-n-alkyl-2-phenylthiophene, and 5-n-alkyl-2-o-tolylthiophene homologous series were synthesized to prove their presence in the pyrolysis products of sulfur-rich kerogen. A study of the pyrolysis products of sulfur-vulcanized polybutadiene confirmed that these compounds can be formed via the thermal transformation of n-alkyl polysulfur-bound fragments of sulfur-rich kerogen. The earlier proposed scheme that assumes the dependence of the composition of the pyrolysis products of sulfur-rich kerogen on its saturation with sulfide bridges was experimentally corroborated. Nauka/Interperiodica 2007.

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