N-cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide

98%

Reagent Code: #91013
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CAS Number 827614-68-6

science Other reagents with same CAS 827614-68-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 287.16 g/mol
Formula C₁₆H₂₂BNO₃
badge Registry Numbers
MDL Number MFCD05663848
thermostat Physical Properties
Melting Point 212-214°C
Boiling Point 444.1°C
inventory_2 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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inventory 1g
10-20 days ฿16,630.00

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N-cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide
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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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