5-Acetylthiophene-2-boronic acid pinacol ester

98%

Reagent Code: #136862
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CAS Number 942070-32-8

science Other reagents with same CAS 942070-32-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 252.14 g/mol
Formula C₁₂H₁₇BO₃S
badge Registry Numbers
MDL Number MFCD08063138
inventory_2 Storage & Handling
Storage Dry, seal, 2-8℃

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient and selective carbon-carbon bond formation under mild conditions. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry for constructing biaryl systems. The thiophene moiety enhances electronic properties, making it valuable in organic semiconductors and sensor applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,400.00
inventory 5g
10-20 days ฿2,656.50

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5-Acetylthiophene-2-boronic acid pinacol ester
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient and selective carbon-carbon bond formation under mild conditions. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry for constructing biaryl systems. The thiophene moiety enhances electronic properties, making it valuable in

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex organic molecules, particularly in pharmaceutical and agrochemical research. Its boronic ester group facilitates efficient and selective carbon-carbon bond formation under mild conditions. Commonly employed in the development of conjugated materials for optoelectronics and in medicinal chemistry for constructing biaryl systems. The thiophene moiety enhances electronic properties, making it valuable in organic semiconductors and sensor applications.

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