(5-Cyanothiophen-2-yl)boronic acid

97%

Reagent Code: #90901
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CAS Number 305832-67-1

science Other reagents with same CAS 305832-67-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.97 g/mol
Formula C₅H₄BNO₂S
thermostat Physical Properties
Melting Point 175°C
Boiling Point 369.3°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(5-Cyanothiophen-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the synthesis of biologically active compounds. Additionally, it is utilized in the development of organic electronic materials, such as polymers and small molecules, for applications in optoelectronics and sensors. Its versatility and reactivity make it a crucial component in modern synthetic chemistry.

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Test Parameter Specification
APPEARANCE White to light brown Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿378.00
inventory 1g
10-20 days ฿945.00

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(5-Cyanothiophen-2-yl)boronic acid
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(5-Cyanothiophen-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the synthesis of biologically active compounds. Ad

(5-Cyanothiophen-2-yl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules. The compound serves as a key intermediate in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group facilitates efficient coupling with aryl halides, making it valuable in the synthesis of biologically active compounds. Additionally, it is utilized in the development of organic electronic materials, such as polymers and small molecules, for applications in optoelectronics and sensors. Its versatility and reactivity make it a crucial component in modern synthetic chemistry.

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