3-(5-Bromothiophen-2-yl)acrylic acid

95%

Reagent Code: #153256
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CAS Number 29079-97-8

science Other reagents with same CAS 29079-97-8

blur_circular Chemical Specifications

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Weight 233.08 g/mol
Formula C₇H₅BrO₂S
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its structure supports conjugation and functionalization, making it valuable in organic synthesis for constructing heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form C–C bonds, enabling the preparation of complex molecules for drug discovery and materials science. Also utilized in the design of organic semiconductors and optoelectronic materials due to the electron-rich nature of the thiophene ring.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,690.00
inventory 250mg
10-20 days ฿2,870.00
inventory 1g
10-20 days ฿8,360.00
inventory 10g
10-20 days ฿57,570.00

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3-(5-Bromothiophen-2-yl)acrylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its structure supports conjugation and functionalization, making it valuable in organic synthesis for constructing heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form C–C bonds, enabling the preparation of complex molecules for drug discovery and materials science. Also utilized in the design of organi

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active compounds. Its structure supports conjugation and functionalization, making it valuable in organic synthesis for constructing heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki and Heck reactions to form C–C bonds, enabling the preparation of complex molecules for drug discovery and materials science. Also utilized in the design of organic semiconductors and optoelectronic materials due to the electron-rich nature of the thiophene ring.

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