2-Bromo-3-octylthiophene

97%

Reagent Code: #142950
label
Alias 2-Bromo-3-octylthiophene
fingerprint
CAS Number 145543-83-5

science Other reagents with same CAS 145543-83-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 275.25 g/mol
Formula C₁₂H₁₉BrS
badge Registry Numbers
MDL Number MFCD13193238
inventory_2 Storage & Handling
Density 1.206
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its alkyl side chain enhances solubility in organic solvents, facilitating solution-processing techniques like spin coating and inkjet printing. The bromine atom allows for further functionalization via cross-coupling reactions, such as Stille or Suzuki coupling, enabling the construction of complex conjugated systems. Commonly employed in the development of semiconducting materials with tunable electronic properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿186.00
inventory 5g
10-20 days ฿920.00
inventory 25g
10-20 days ฿2,189.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Bromo-3-octylthiophene
No image available

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its alkyl side chain enhances solubility in organic solvents, facilitating solution-processing techniques like spin coating and inkjet printing. The bromine atom allows for further functionalization via cross-coupling reactions, such as Stille or Suzuki coupling, enabling the construction of complex conjugated systems. Commo

Used as a key intermediate in the synthesis of conjugated polymers for organic electronics, particularly in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its alkyl side chain enhances solubility in organic solvents, facilitating solution-processing techniques like spin coating and inkjet printing. The bromine atom allows for further functionalization via cross-coupling reactions, such as Stille or Suzuki coupling, enabling the construction of complex conjugated systems. Commonly employed in the development of semiconducting materials with tunable electronic properties.

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...