(3-(Diisopropylcarbamoyl)phenyl)boronic acid
97%
Reagent
Code: #90028
CAS Number
850567-40-7
blur_circular Chemical Specifications
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Molecular Information
Weight
249.12 g/mol
Formula
C₁₃H₂₀BNO₃
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Registry Numbers
MDL Number
MFCD06659890
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Physical Properties
Melting Point
170-174 °C
Boiling Point
441.2 °C at 760 mmHg
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Storage & Handling
Storage
room temperature, inert gas storage
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic acid reagent, enabling the formation of carbon-carbon bonds, which is essential in the production of pharmaceuticals, agrochemicals, and advanced materials. Its diisopropylcarbamoyl group enhances its stability and reactivity, making it suitable for complex molecular constructions. Additionally, it finds application in the development of sensors and catalysts due to its ability to interact with various organic and inorganic substrates.
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