N-cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
98%
Reagent
Code: #91013
CAS Number
827614-68-6
science Other reagents with same CAS 827614-68-6
blur_circular Chemical Specifications
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Molecular Information
Weight
287.16 g/mol
Formula
C₁₆H₂₂BNO₃
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Registry Numbers
MDL Number
MFCD05663848
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Physical Properties
Melting Point
212-214°C
Boiling Point
444.1°C
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Storage & Handling
Density
1.11g/mL
Storage
2-8°C
description Product Description
Used in organic synthesis as a key intermediate for the preparation of various pharmaceuticals and biologically active compounds. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the synthesis of complex molecules. Its boronate ester group makes it highly reactive and selective in coupling reactions, often employed in the development of drug candidates and agrochemicals. Additionally, it serves as a building block in medicinal chemistry for creating compounds with potential therapeutic properties, such as enzyme inhibitors or receptor modulators. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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