5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene

95%

Reagent Code: #162583
fingerprint
CAS Number 219537-97-0

science Other reagents with same CAS 219537-97-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.31 g/mol
Formula C₁₅H₁₄Cl₂S₂
badge Registry Numbers
MDL Number MFCD19382349
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance organic thin-film transistors (OTFTs) and organic photovoltaics (OPVs). Its structure featuring two chlorine-substituted methylthiophene units linked by a cyclopentene ring enhances π-π stacking and improves charge carrier mobility, making it valuable in flexible electronics and printable circuits. Commonly employed in research and development of donor-acceptor type conjugated polymers for use in solar cells and sensors due to its favorable electronic properties and thermal stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,280.00
inventory 250mg
10-20 days ฿6,520.00
inventory 1g
10-20 days ฿16,290.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Chloro-3-[2-(5-chloro-2-methylthien-3-yl)cyclopent-1-en-1-yl]-2-methylthiophene
No image available

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance organic thin-film transistors (OTFTs) and organic photovoltaics (OPVs). Its structure featuring two chlorine-substituted methylthiophene units linked by a cyclopentene ring enhances π-π stacking and improves charge carrier mobility, making it valuable in flexible electronics and printable circuits. Commonly employed in research and development of donor-acceptor type conjugated polyme

Used as a key intermediate in the synthesis of organic semiconductors, particularly in the development of high-performance organic thin-film transistors (OTFTs) and organic photovoltaics (OPVs). Its structure featuring two chlorine-substituted methylthiophene units linked by a cyclopentene ring enhances π-π stacking and improves charge carrier mobility, making it valuable in flexible electronics and printable circuits. Commonly employed in research and development of donor-acceptor type conjugated polymers for use in solar cells and sensors due to its favorable electronic properties and thermal stability.

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...