Cyclohexylboronic acid

97%

Reagent Code: #91174
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Alias Cyclohexylboronic acid
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CAS Number 4441-56-9

science Other reagents with same CAS 4441-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 127.98 g/mol
Formula C₆H₁₃BO₂
badge Registry Numbers
MDL Number MFCD01311824
thermostat Physical Properties
Melting Point 122-123 °C
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Cyclohexylboronic 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. It serves as a key reagent in the synthesis of complex organic molecules, enabling the introduction of cyclohexyl groups into target compounds. Additionally, it is utilized in the development of bioactive compounds and in research for drug discovery, where precise molecular modifications are required. Its stability and reactivity make it a versatile tool in modern synthetic chemistry.

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Test Parameter Specification
Purity (Neutralization Titration) 97-103
Appearance White to yellow powder, crystals, and/or chunks
Infrared Spectrum Conforms to Structure
Proton NMR Spectrum Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,380.00
inventory 25g
10-20 days ฿6,860.00

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Cyclohexylboronic acid
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Cyclohexylboronic 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. It serves as a key reagent in the synthesis of complex organic molecules, enabling the introduction of cyclohexyl groups into target compounds. Additionally, it is utilized in the development of bioactive compounds and in research for drug discovery, where precise molecular modifications are required. Its stability and reactivity make it a versatile tool in modern synthetic chemistry.
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