2-Bromothiophene Property

Melting point:

-10 °C

Boiling point:

149-151 °C (lit.)

Density 

1.684 g/mL at 25 °C (lit.)

refractive index 

n20/D 1.586(lit.)

Flash point:

140 °F

storage temp. 

2-8°C

form 

Liquid

color 

Clear colorless to slightly brownish

Specific Gravity

1.684

Water Solubility 

IMMISCIBLE

Sensitive 

Light Sensitive

BRN 

104663

InChIKey

TUCRZHGAIRVWTI-UHFFFAOYSA-N

CAS DataBase Reference

1003-09-4(CAS DataBase Reference)

NIST Chemistry Reference

Thiophene, 2-bromo-(1003-09-4)

EPA Substance Registry System

Thiophene, 2-bromo- (1003-09-4)

Safety

Hazard Codes 

T,N,Xn

Risk Statements 

10-25-41-51/53-36/37/38-23/24-22-20/21/22

Safety Statements 

26-36/37/39-45-61-16-36

RIDADR 

UN 2929 6.1/PG 2

WGK Germany 

3

F 

8

Hazard Note 

Irritant

TSCA 

T

HazardClass 

6.1

PackingGroup 

II

HS Code 

29349990

Hazard and Precautionary Statements (GHS)

Symbol(GHS)

Signal word

Danger

Hazard statements

H226Flammable liquid and vapour

H300Fatal if swallowed

H318Causes serious eye damage

Precautionary statements

P210Keep away from heat/sparks/open flames/hot surfaces. — No smoking.

P233Keep container tightly closed.

P240Ground/bond container and receiving equipment.

P280Wear protective gloves/protective clothing/eye protection/face protection.

P301+P310IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician.

P305+P351+P338IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continuerinsing.

2-Bromothiophene Chemical Properties,Usage,Production

General description

2-Bromothiophene undergoes metallation-alkylation reaction with various electrophiles to generate various 5-alkylated 2-bromo products. It is coupled with 4-bromoallyl phenyl ether to produce allyl thiophene ether, which is a new type of organic thin film transistor dielectric material.

Application

In dimethylformamide containing tetramethylammonium perchlorate, 2-bromothiophene is electrochemically reduced many mono- and dihalothiophenes on a carbon cathode by cyclic voltammetry and controlled potential electrolysis.

Product Introduction

The 2-Bromothiophene(casno:1003-09-4) is an organic compound with the formula C4H3BrS. The IUPAC name of this chemical is 2-bromothiophene. With the CAS registry number 1003-09-4, it is also named as Bromothiophene. The product's categories are Thiophenes; Halides; Thiophenes & Benzothiophenes; Thiophene & Benzothiophene; Thiophenes & Benzothiophenes. Besides, 2-Bromothiophene(casno:1003-09-4) is a colorless to light yellow transparent liquid, which should be stored in a closed dark and cool place. 2-Bromothiophene(casno:1003-09-4) can be used for organic synthesis and pharmaceutical intermediates.

Chemical Properties

colorless to light yellow liquid. Soluble in ether and acetone, insoluble in water.

Uses

2-Bromothiophene has been used in electrochemical reduction of a number of mono- and dihalothiophenes at carbon cathodes in dimethylformamide containing tetramethylammonium per chlorate by cyclic voltammetry and controlled-potential electrolysis.

Preparation

2-Bromothiophene is synthesized by bromination of thiophene, which is achieved through the following steps: dissolve thiophene in acetic acid, and add bromine in glacial acetic acid solution below 10°C. Water was added to the reaction mixture to precipitate an oily liquid. Extract with ether. Add potassium carbonate to the extract to remove acetic acid, dry it, distill off the ether, and then conduct vacuum distillation to collect fractions at 42-46°C (1.73kPa) to obtain 2-bromothiophene with a yield of 55%.

Synthesis Reference(s)

Journal of the American Chemical Society, 79, p. 5474, 1957 DOI: 10.1021/ja01577a039
Synthesis, p. 890, 1988 DOI: 10.1055/s-1988-27740

General Description

2-Bromothiophene undergoes metalation-alkylation reaction with various electrophiles to form various 5-alkylated 2-bromo products. It undergoes coupling with 4-bromo allyl phenyl ether to form allyl phenyl thiophene ether, which is a novel potential dielectric material for organic thin film transistors.