Ethyl 2-bromothieno[3,2-b]thiophene-3-carboxylate

98%

Reagent Code: #184667
fingerprint
CAS Number 2055722-78-4

science Other reagents with same CAS 2055722-78-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 291.19 g/mol
Formula C₉H₇BrO₂S₂
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

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 backbone enables efficient palladium-catalyzed cross-coupling reactions, facilitating the construction of complex π-conjugated systems. The compound is valued for enhancing charge carrier mobility and thermal stability in thin-film electronic devices. It also finds use in the preparation of donor-acceptor type copolymers due to its electron-withdrawing ester group and rigid planar structure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿22,090.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 2-bromothieno[3,2-b]thiophene-3-carboxylate
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 backbone enables efficient palladium-catalyzed cross-coupling reactions, facilitating the construction of complex π-conjugated systems. The compound is valued for enhancing charge carrier mobility and thermal stability in thin-film electronic devices. It also finds use in the pr

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 backbone enables efficient palladium-catalyzed cross-coupling reactions, facilitating the construction of complex π-conjugated systems. The compound is valued for enhancing charge carrier mobility and thermal stability in thin-film electronic devices. It also finds use in the preparation of donor-acceptor type copolymers due to its electron-withdrawing ester group and rigid planar structure.

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...