4-Chloro-3-(cyclohexylaminocarbonyl)phenylboronic acid

98%

Reagent Code: #90636
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CAS Number 871332-92-2

science Other reagents with same CAS 871332-92-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.54 g/mol
Formula C₁₃H₁₇BClNO₃
badge Registry Numbers
MDL Number MFCD07783884
thermostat Physical Properties
Melting Point 252-256°C
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it may be employed in the development of sensors or probes due to its ability to interact with diols and other functional groups, facilitating applications in analytical chemistry and biochemical research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,780.00
inventory 1g
10-20 days ฿7,320.00

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4-Chloro-3-(cyclohexylaminocarbonyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the formation of carbon-carbon bonds, enabling the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group allows for efficient coupling with aryl halides, making it valuable in the production of biaryl compounds. Additionally, it may be employed in the development of sensors or probes due to its ability to interact with diols and other functional groups, facilitating applications in analytical chemistry and biochemical research.
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