N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclohexanecarboxamide

95%

Reagent Code: #83831
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CAS Number 2246818-94-8

science Other reagents with same CAS 2246818-94-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.250 g/mol
Formula C₁₉H₂₈BNO₃
badge Registry Numbers
MDL Number MFCD14585588
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of medicinal chemistry. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound’s structure, featuring a cyclohexane moiety, contributes to its potential use in designing molecules with specific steric and electronic properties, which can be crucial for drug discovery and optimization. Its applications also extend to the synthesis of boron-containing compounds, which are increasingly relevant in areas such as cancer therapy and imaging agents.

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Test Parameter Specification
Appearance White Powder
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,940.00
inventory 1g
10-20 days ฿43,200.00

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N-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]cyclohexanecarboxamide
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This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of medicinal chemistry. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound’s structure, featuring a cyclohexane moiety, contr

This compound is primarily utilized in organic synthesis as a key intermediate in the preparation of more complex molecules, particularly in the field of medicinal chemistry. Its boronate ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This reaction is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, the compound’s structure, featuring a cyclohexane moiety, contributes to its potential use in designing molecules with specific steric and electronic properties, which can be crucial for drug discovery and optimization. Its applications also extend to the synthesis of boron-containing compounds, which are increasingly relevant in areas such as cancer therapy and imaging agents.

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