2-bromo-3-(2-(2-bromothiophen-3-yl)phenyl)thiophene

97%

Reagent Code: #150151
fingerprint
CAS Number 2181002-18-4

science Other reagents with same CAS 2181002-18-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 400.15 g/mol
Formula C₁₄H₈Br₂S₂
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated thiophene structure enables efficient cross-coupling reactions, such as Suzuki or Stille couplings, allowing for precise construction of complex π-conjugated systems. The compound’s rigid, planar backbone enhances charge carrier mobility in thin-film electronic devices. It is also employed in the preparation of low-bandgap polymers that absorb light in the near-infrared region, making it valuable for use in solar cells and photodetectors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿19,000.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-bromo-3-(2-(2-bromothiophen-3-yl)phenyl)thiophene
No image available

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated thiophene structure enables efficient cross-coupling reactions, such as Suzuki or Stille couplings, allowing for precise construction of complex π-conjugated systems. The compound’s rigid, planar backbone enhances charge carrier mobility in thin-film electronic devices. It is also employe

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its brominated thiophene structure enables efficient cross-coupling reactions, such as Suzuki or Stille couplings, allowing for precise construction of complex π-conjugated systems. The compound’s rigid, planar backbone enhances charge carrier mobility in thin-film electronic devices. It is also employed in the preparation of low-bandgap polymers that absorb light in the near-infrared region, making it valuable for use in solar cells and photodetectors.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...