2,5-Dibromo-3-hexadecylthiophene

≥96%

Reagent Code: #174375
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CAS Number 178452-13-6

science Other reagents with same CAS 178452-13-6

blur_circular Chemical Specifications

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Weight 466.36 g/mol
Formula C₂₀H₃₄Br₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of conjugated polymers for organic semiconductors. It plays an important role in the development of organic field-effect transistors (OFETs) and organic photovoltaics (OPVs) due to its ability to enhance charge carrier mobility and film stability. The long hexadecyl chain improves solubility in organic solvents, facilitating solution-processing techniques like spin coating and inkjet printing. Its brominated structure allows for further functionalization via cross-coupling reactions, making it valuable in tailoring electronic properties of π-conjugated systems.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿2,240.00
inventory 5g
10-20 days ฿25,590.00
inventory 1g
10-20 days ฿6,190.00

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2,5-Dibromo-3-hexadecylthiophene
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Used as a key intermediate in the synthesis of conjugated polymers for organic semiconductors. It plays an important role in the development of organic field-effect transistors (OFETs) and organic photovoltaics (OPVs) due to its ability to enhance charge carrier mobility and film stability. The long hexadecyl chain improves solubility in organic solvents, facilitating solution-processing techniques like spin coating and inkjet printing. Its brominated structure allows for further functionalization via cr

Used as a key intermediate in the synthesis of conjugated polymers for organic semiconductors. It plays an important role in the development of organic field-effect transistors (OFETs) and organic photovoltaics (OPVs) due to its ability to enhance charge carrier mobility and film stability. The long hexadecyl chain improves solubility in organic solvents, facilitating solution-processing techniques like spin coating and inkjet printing. Its brominated structure allows for further functionalization via cross-coupling reactions, making it valuable in tailoring electronic properties of π-conjugated systems.

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