210705-84-3

Basic information

• Product Name: 2-BroMo-4-hexylthiophene
• Synonyms: 2-BroMo-4-hexylthiophene;2-Bromo-4-hexylthiophene 97%
• CAS NO: 210705-84-3
• Molecular Formula: C10H15BrS
• Molecular Weight: 247.1951
• EINECS: -0
• Mol File: 210705-84-3.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 144°C/10mmHg(lit.)
• Appearance: /
• Density: 1.2225 g/mL at 25 °C
• Refractive Index: n20/D1.5265
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 2-BroMo-4-hexylthiophene(CAS DataBase Reference)
• NIST Chemistry Reference: 2-BroMo-4-hexylthiophene(210705-84-3)
• EPA Substance Registry System: 2-BroMo-4-hexylthiophene(210705-84-3)

Safety Data

• Hazard Codes: T
• Statements: 25
• Safety Statements: 45
• RIDADR: UN 2810 6.1 / PGIII
• WGK Germany: 3
• Hazardous Substances Data: 210705-84-3(Hazardous Substances Data)

Usage

General Description

2-Bromo-4-hexylthiophene is a chemical compound with the molecular formula C10H15BrS. It is a brominated derivative of hexylthiophene, which belongs to the family of thiophene compounds. This chemical is commonly used in organic electronic materials and has potential applications in organic photovoltaics, organic light-emitting diodes, and organic field-effect transistors. Its unique properties make it suitable for use in the fabrication of thin-film transistors and other organic electronic devices. 2-Bromo-4-hexylthiophene is known for its high thermal stability, good solubility, and efficient charge transport characteristics, making it a valuable material in the field of organic electronics.

Upstream product

• 1693-86-3 3-hexylthiophene 
• 1196663-02-1 (5-bromo-3-hexylthiophen-2-yl)magnesium chloride 

Downstream Products

• 135926-93-1 3,4'-dihexyl-2,2'-bithiophene 
• 1350826-98-0 C₂₈H₂₇NS 

Relevant articles and documents

Effect of structural modification on the performances of phenothiazine-dye sensitized solar cells

Three novel dyes DX1, DX2 and DX3 containing phenothiazine are designed and synthesized for dye-sensitized solar cells (DSSCs). Photophysical, electrochemical and photovoltaic properties of the three dyes have been systematically investigated. The results

LiCl-promoted chain growth kumada catalyst-transfer polycondensation of the "reversed" thiophene monomer

The effect of LiCl on the chain growth Kumada catalyst-transfer polycondensation (KCTP) of the "reversed" thiophene monomer, 5-bromo-2-chloromagnesio-3-hexylthiophene (3a) (that has bulky substituent adjacent to the chloromagnesium group), was investigate

A selective and direct synthesis of 2-bromo-4-alkylthiophenes: Convenient and straightforward approaches for the synthesis of head-to-tail (HT) and tail-to-tail (TT) dihexyl-2,2′-bithiophenes

A straightforward method for the synthesis of 2-bromo-4-alkylthiophenes was developed, and the desired products were obtained in the highest chemical yields (>90%) reported to date. 2-Bromo-4-alkylthiophenes were synthesized by regioselective lithiating of 3-alkylthiophenes with n-BuLi and quenching with bromine at -78°C. Moreover, a simple and efficient protocol for the synthesis of dihexyl-2,2′-bithiophenes was developed by employing 2-bromo-4-hexylthiophene instead of the commonly used monomer, 2-bromo-3-hexylthiophene. Kumada and Suzuki cross-coupling reactions were conducted to synthesize the desired products as head-to-tail (HT) and tail-to-tail (TT) regioisomers in high yields and excellent selectivity.