(3-Chloro-4-(cyclohexylcarbamoyl)- phenyl)boronic acid

98%

Reagent Code: #90206
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CAS Number 957034-65-0

science Other reagents with same CAS 957034-65-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.55 g/mol
Formula C₁₃H₁₇BClNO₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in material science for designing advanced polymers and functional materials. Its cyclohexylcarbamoyl moiety contributes to enhancing the stability and specificity of the resulting compounds, making it valuable in targeted applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,620.00
inventory 1g
10-20 days ฿4,340.00

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(3-Chloro-4-(cyclohexylcarbamoyl)- phenyl)boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in material science for designing advanced polymers and fun

This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex organic molecules, especially in the pharmaceutical industry, where it aids in the development of drugs and bioactive compounds. Its boronic acid group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in material science for designing advanced polymers and functional materials. Its cyclohexylcarbamoyl moiety contributes to enhancing the stability and specificity of the resulting compounds, making it valuable in targeted applications.

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