[4-(cyclopentylcarbamoyl)phenyl]boronic acid

95%

Reagent Code: #162329
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CAS Number 850568-15-9

science Other reagents with same CAS 850568-15-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.0713 g/mol
Formula C₁₂H₁₆BNO₃
badge Registry Numbers
MDL Number MFCD03788418
thermostat Physical Properties
Melting Point 196-200 °C
inventory_2 Storage & Handling
Density 1.21 g/cm3
Storage 2-8°C, dry

description Product Description

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in the preparation of complex aromatic compounds. Commonly employed in medicinal chemistry for constructing biaryl systems found in bioactive molecules. Also utilized in the synthesis of potential drug candidates targeting proteases and kinases due to its ability to enhance binding interactions. Stable under various reaction conditions, it supports high-yield transformations with good functional group tolerance.

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inventory 1g
10-20 days ฿3,300.00

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[4-(cyclopentylcarbamoyl)phenyl]boronic acid
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Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in the preparation of complex aromatic compounds. Commonly employed in medicinal chemistry for constructing biaryl systems found in bioactive molecules. Also utilized in the synthesis of potential drug candidates targeting pr

Used in organic synthesis as a building block for Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical development. Its boronic acid functionality allows for efficient coupling with aryl halides, making it valuable in the preparation of complex aromatic compounds. Commonly employed in medicinal chemistry for constructing biaryl systems found in bioactive molecules. Also utilized in the synthesis of potential drug candidates targeting proteases and kinases due to its ability to enhance binding interactions. Stable under various reaction conditions, it supports high-yield transformations with good functional group tolerance.

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