Quinolin-6-yl-6-boronic acid

≥97%

Reagent Code: #91026
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CAS Number 376581-24-7

science Other reagents with same CAS 376581-24-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 172.98 g/mol
Formula C₉H₈BNO₂
badge Registry Numbers
MDL Number MFCD03093100
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

Quinolin-6-yl-6-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with specific biological targets.

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Test Parameter Specification
Appearance White to Off-white Powder
Purity (%) 97-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,258.00
inventory 5g
10-20 days ฿8,028.00

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Quinolin-6-yl-6-boronic acid
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Quinolin-6-yl-6-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the crea

Quinolin-6-yl-6-boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules, including drug candidates and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the creation of diverse chemical structures. Additionally, it is employed in the development of sensors and diagnostic tools due to its ability to interact with specific biological targets.

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