[4-(prop-2-en-1-ylcarbamoyl)phenyl]boronic acid
98%
Reagent
Code: #90667
CAS Number
850568-20-6
science Other reagents with same CAS 850568-20-6
blur_circular Chemical Specifications
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Molecular Information
Weight
205 g/mol
Formula
C₁₀H₁₂BNO₃
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Registry Numbers
MDL Number
MFCD04115674
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Physical Properties
Melting Point
196-200℃
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Storage & Handling
Density
1.18±0.1 g/cm3
Storage
Dry, sealed, 2-8℃
description Product Description
This chemical is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it acts as a key intermediate for producing biaryl compounds. These reactions are essential in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group enables efficient coupling with aryl halides, making it valuable for constructing complex organic molecules. Additionally, it finds applications in the preparation of polymer materials and as a building block for synthesizing bioactive compounds in medicinal chemistry research. Its versatility and reactivity make it a crucial component in modern synthetic chemistry workflows.
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