2-Bromo-5-iodothiophene

98%

Reagent Code: #150026
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CAS Number 29504-81-2

science Other reagents with same CAS 29504-81-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 288.93 g/mol
Formula C₄H₂BrIS
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MDL Number MFCD08695058
inventory_2 Storage & Handling
Storage 2-8°C, avoid light, inert gas storage

description Product Description

Used as an intermediate in the synthesis of conjugated polymers and organic semiconductors for electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its halogen substituents allow for selective cross-coupling reactions, particularly in Suzuki and Stille couplings, enabling the construction of complex π-conjugated systems. Also employed in the development of pharmaceuticals and agrochemicals where thiophene derivatives exhibit biological activity. Its reactivity makes it valuable in forming carbon-carbon bonds during the preparation of advanced organic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿730.00
inventory 250mg
10-20 days ฿1,650.00
inventory 1g
10-20 days ฿4,210.00
inventory 5g
10-20 days ฿14,310.00

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2-Bromo-5-iodothiophene
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Used as an intermediate in the synthesis of conjugated polymers and organic semiconductors for electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its halogen substituents allow for selective cross-coupling reactions, particularly in Suzuki and Stille couplings, enabling the construction of complex π-conjugated systems. Also employed in the development of pharmaceuticals and agrochemicals where thiophene derivatives exhibit biological activity. Its reacti

Used as an intermediate in the synthesis of conjugated polymers and organic semiconductors for electronic devices such as organic field-effect transistors (OFETs) and organic photovoltaics (OPVs). Its halogen substituents allow for selective cross-coupling reactions, particularly in Suzuki and Stille couplings, enabling the construction of complex π-conjugated systems. Also employed in the development of pharmaceuticals and agrochemicals where thiophene derivatives exhibit biological activity. Its reactivity makes it valuable in forming carbon-carbon bonds during the preparation of advanced organic materials.

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