392662-65-6

Basic information

• Product Name: 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE
• Synonyms: 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE
• CAS NO: 392662-65-6
• Molecular Formula: C₆H₂Br₂S₂
• Molecular Weight: 298.03
• Product Categories: Heterocycle-oher series
• Mol File: 392662-65-6.mol
• Article Data: 1

Chemical Properties

• Melting Point: 127 °C
• Boiling Point: 332.409 °C at 760 mmHg
• Flash Point: 154.836 °C
• Appearance: /
• Density: 2.21 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.774
• Storage Temp.: Refrigerator
• CAS DataBase Reference: 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE(CAS DataBase Reference)
• NIST Chemistry Reference: 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE(392662-65-6)
• EPA Substance Registry System: 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE(392662-65-6)

Safety Data

• Hazardous Substances Data: 392662-65-6(Hazardous Substances Data)

Usage

General Description

3,6-Dibromothieno[3,2-b]thiophene is a chemical compound with the molecular formula C6H3Br2S. It is a dibrominated thiophene derivative, which is a type of heterocyclic compound that contains a five-membered sulfur-containing ring. 3,6-DIBROMOTHIENO[3,2-B]THIOPHENE is commonly used as a building block in the synthesis of various organic molecules, particularly in the field of organic electronics and materials science. Its unique structure and reactivity make it highly valuable for the development of advanced materials, such as organic semiconductors and polymers. Additionally, 3,6-Dibromothieno[3,2-b]thiophene is known for its high thermal stability and potential as a promising candidate for use in optoelectronic devices, such as organic light-emitting diodes and organic photovoltaics.

InChI:InChI=1/C6H2Br2S2/c7-3-1-9-6-4(8)2-10-5(3)6/h1-2H

Upstream product

• 930-96-1 3-bromo-2-thiophenecarboxaldehyde 

Downstream Products

• 1312547-05-9 [(S)-1-((S)-2-{4-[4-(6-bromothieno[3,2-b]thiophen-3-yl)phenyl]-1H-imidazol-2-yl}pyrrolidine-1-carbonyl)-2-methylpropyl]carbamic acid methyl ester 
• 1312547-99-1 (S)-2-{5-[4-(6-bromothieno[3,2-b]thiophen-3-yl)phenyl]-1H-imidazol-2-yl}pyrrolidine-1-carboxylic acid tert-butyl ester 
• 1261434-20-1 3,6-bis(4-trifluoromethylphenyl)thieno[3,2-b]thiophene 
• 1377584-31-0 3,6-bis(4-trifluoromethylphenyl)thieno[3,2-b]thiophene-2,5-dione 
• 1377584-32-1 2,5-bis(dicyanomethylene)-3,6-bis(4-trifluoromethylphenyl)thieno[3,2-b]thiophene 
• 1312547-20-8 [(S)-1-((S)-2-{4-[4-(6-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methylbutyryl)pyrrolidin-2-yl]-3H-benzoimidazol-5-yl}thieno[3,2-b]thiophen-3-yl)phenyl]-1H-imidazol-2-yl}pyrrolidine-1-carbonyl)-2-methylpropyl]carbamic acid methyl ester 
• 1312546-37-4 {(S)-1-[(S)-2-(5-{4-[6-(4-{2-[(S)-1-((S)-2-methoxycarbonylamino-3-methylbutyryl)pyrrolidin-2-yl]-3H-imidazol-4-yl}phenyl)thieno[3,2-b]thiophen-3-yl]phenyl}-1H-imidazol-2-yl)pyrrolidine-1-carbonyl]-2-methylpropyl}carbamicacid methyl ester 
• 1312547-21-9 [(S)-1-((S)-2-{5-[4-(6-{(S)-2-[1-((R)-2-methoxycarbonylamino-2-phenylacetyl)-pyrrolidin-2-yl]-3H-benzoimidazol-5-yl}-thieno[3,2-b]-thiophen-3-yl)-phenyl]-1H-imidazol-2-yl}pyrrolidine-1-carbonyl)-2-methylpropyl]-carbamic acid methyl ester 
• 1492981-39-1 3,6-bis(2-ethylhexylsulfanyl)thieno[3,2-b]thiophene 
• 56412-11-4 3,6-Dimethylthienol<3,2-b>thiophen 
• 1805838-30-5 thieno[3,2-b]thiophene-3,6-dicarboxylic acid 

Relevant articles and documents

A new alkyl substituted and method for the synthesis of polythiophene

The invention provides a method for replacing multi-thiophthene with beta-dialkyl in a synthesis formula I. The method comprises the following steps of: (f) reacting an intermediate in a formula 10 to obtain an intermediate in a formula 11; (g) reacting the intermediate in the formula 11 to obtain an intermediate in a formula 12; (h) reacting the intermediate in the formula 12 to obtain an intermediate in a formula 13; (i) reacting the intermediate in the formula 13 to obtain an intermediate in a formula 8; (j) reacting the intermediate in the formula 8 to obtain an intermediate in a formula 9; and (k) reacting the intermediate in the formula 9 to obtain a compound in a formula I. The invention further relates to the intermediate in the formula 9. The method disclosed by the invention is low in cost, simple in process, high in yield and low in pollution. The formulas 10, 11, 12, 13, 8 and 9 are shown in the description.