3,4-difluoro-2,5-bis(trimethylstannyl)thiophene

99%

Reagent Code: #180315
fingerprint
CAS Number 870718-97-1

science Other reagents with same CAS 870718-97-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 445.736 g/mol
Formula C₁₀H₁₈F₂SSn₂
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

description Product Description

Used primarily as a key intermediate in the synthesis of conjugated polymers for organic electronics. Its stannyl groups enable efficient Stille coupling reactions, making it valuable in creating organic semiconductors for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The fluorine substituents enhance electron affinity and improve charge carrier mobility, contributing to better device performance. It is also employed in the development of thiophene-based copolymers with tunable electronic properties for use in flexible electronics and printable circuits.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿16,900.00
inventory 1g
10-20 days ฿40,000.00
inventory 100mg
10-20 days ฿11,270.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3,4-difluoro-2,5-bis(trimethylstannyl)thiophene
No image available

Used primarily as a key intermediate in the synthesis of conjugated polymers for organic electronics. Its stannyl groups enable efficient Stille coupling reactions, making it valuable in creating organic semiconductors for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The fluorine substituents enhance electron affinity and improve charge carrier mobility, contributing to better device performance. It is also employed in the development of thiophene-based copol

Used primarily as a key intermediate in the synthesis of conjugated polymers for organic electronics. Its stannyl groups enable efficient Stille coupling reactions, making it valuable in creating organic semiconductors for applications in organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). The fluorine substituents enhance electron affinity and improve charge carrier mobility, contributing to better device performance. It is also employed in the development of thiophene-based copolymers with tunable electronic properties for use in flexible electronics and printable circuits.

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...