4-Bromo-7-(5'-hexyl-[2,2'-bithiophen]-5-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine

98%

Reagent Code: #154650
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CAS Number 1361034-02-7

science Other reagents with same CAS 1361034-02-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 464.47 g/mol
Formula C₁₉H₁₈BrN₃S₃
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a key intermediate in organic semiconductors, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its structure supports strong π-π stacking and charge carrier mobility, making it valuable in developing high-performance electronic materials. Commonly employed in donor-acceptor type copolymers to tune bandgap and enhance device efficiency. Also utilized in research settings for designing novel thiophene-based functional materials with improved thermal and environmental stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿10,730.00
250mg
10-20 days ฿18,220.00
1g
10-20 days ฿60,340.00
4-Bromo-7-(5'-hexyl-[2,2'-bithiophen]-5-yl)-[1,2,5]thiadiazolo[3,4-c]pyridine
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Used as a key intermediate in organic semiconductors, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its structure supports strong π-π stacking and charge carrier mobility, making it valuable in developing high-performance electronic materials. Commonly employed in donor-acceptor type copolymers to tune bandgap and enhance device efficiency. Also utilized in research settings for designing novel thiophene-based functiona

Used as a key intermediate in organic semiconductors, particularly in the synthesis of conjugated polymers for organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its structure supports strong π-π stacking and charge carrier mobility, making it valuable in developing high-performance electronic materials. Commonly employed in donor-acceptor type copolymers to tune bandgap and enhance device efficiency. Also utilized in research settings for designing novel thiophene-based functional materials with improved thermal and environmental stability.

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