2,2'-BITHIOPHENE

Defined Molecular Structure: Contains two thiophene rings linked through their 2-positions.

Conjugated Structure: Features an extended π-conjugated molecular system.

Organic Synthesis Building Block: Suitable for preparing functional thiophene derivatives.

Material Research Potential: Relevant to organic electronic and semiconductor material research.

 Polymer Research Application: Can serve as a starting material for thiophene-based conjugated polymers.

Versatile Research Intermediate: Used in heterocyclic chemistry and specialty organic material development.

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2,2'-BITHIOPHENE CAS#492-97-7 Chemical Properties

Melting point 

32-33 °C (lit.)

Boiling point 

260 °C (lit.)

density 

1.2455 (rough estimate)

refractive index 

1.6210 (estimate)

Fp 

>230 °F

storage temp. 

Keep in dark place,Inert atmosphere,Room temperature

form 

powder to lump to clear liquid

color 

White or Colorless to Light yellow to Green

Water Solubility 

Insoluble in water.

Sensitive 

Light Sensitive

BRN 

3039

InChIKey

OHZAHWOAMVVGEL-UHFFFAOYSA-N

LogP

3.750

CAS DataBase Reference

492-97-7(CAS DataBase Reference)

EPA Substance Registry System

2,2'-Bithiophene (492-97-7)

Safety Information

Hazard Codes 

Xi,Xn

Risk Statements 

20/21/22-36/37/38

Safety Statements 

22-24/25-36-26

WGK Germany 

3

F 

10-23

TSCA 

T

HazardClass 

IRRITANT

HS Code 

29309090

Product Overview

2,2'-Bithiophene is a sulfur-containing heterocyclic aromatic compound consisting of two thiophene rings connected by a carbon-carbon bond at their 2-positions. Its conjugated molecular structure makes it an important building block in organic synthesis and functional materials research.

The compound is commonly used as an intermediate for preparing substituted bithiophenes, oligothiophenes, and other thiophene-based derivatives. It is also relevant to research involving organic semiconductors, conductive polymers, and organic electronic materials.

2,2'-Bithiophene

 

Product Manufacturing Process

2,2'-Bithiophene can be prepared through chemical coupling approaches involving thiophene-based starting materials. Following the reaction, the product is isolated, purified, and tested according to the required quality specifications.

The specific manufacturing route and purification conditions depend on the manufacturer's process.

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