(5-(Ethoxycarbonyl)thiophen-3-yl)boronic acid

96%

Reagent Code: #185418
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CAS Number 957121-19-6

science Other reagents with same CAS 957121-19-6

blur_circular Chemical Specifications

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Weight 200 g/mol
Formula C₇H₉BO₄S
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical industries. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly applied in the development of conjugated organic materials, including semiconductors and fluorescent dyes. Also utilized in medicinal chemistry for constructing heterocyclic scaffolds found in bioactive molecules. The ethoxycarbonyl group enhances solubility and provides a handle for further functionalization. Stable enough for storage but reactive under standard palladium-catalyzed coupling conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,190.00
inventory 250mg
10-20 days ฿3,720.00
(5-(Ethoxycarbonyl)thiophen-3-yl)boronic acid
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical industries. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly applied in the development of conjugated organic materials, including semiconductors and fluorescent dyes. Also utilized in medicinal chemistry for constructing heterocyclic scaffolds found in bioactive molecules. The ethoxycarbonyl group enhances solu

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions for the synthesis of biaryl compounds in pharmaceutical and agrochemical industries. Its boronic acid group enables efficient carbon-carbon bond formation under mild conditions. Commonly applied in the development of conjugated organic materials, including semiconductors and fluorescent dyes. Also utilized in medicinal chemistry for constructing heterocyclic scaffolds found in bioactive molecules. The ethoxycarbonyl group enhances solubility and provides a handle for further functionalization. Stable enough for storage but reactive under standard palladium-catalyzed coupling conditions.

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