(3-((4-Methoxyphenyl)carbamoyl)phenyl)boronic acid

98%

Reagent Code: #65439
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CAS Number 874459-99-1

science Other reagents with same CAS 874459-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.08 g/mol
Formula C₁₄H₁₄BNO₄
badge Registry Numbers
MDL Number MFCD28167459
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 boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its methoxyphenyl group enhances stability and reactivity, making it suitable for constructing complex organic molecules. Additionally, it finds applications in the development of bioactive compounds and as an intermediate in the synthesis of organic electronic materials.

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Test Parameter Specification
Appearance Off-White Solid
Purity (%) 94.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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inventory 1g
10-20 days ฿25,700.00

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(3-((4-Methoxyphenyl)carbamoyl)phenyl)boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds between aryl or vinyl groups. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its methoxyphenyl group enhances stability and reactivity, making it suitable for constructing complex organic molecules. Additionally, it finds applications in the development of bioactive compounds and as an intermediate in the synthesis of organic electronic materials.
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