N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide

≥98%

Reagent Code: #91019
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CAS Number 616880-14-9

science Other reagents with same CAS 616880-14-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.18 g/mol
Formula C₁₃H₂₀BNO₄S
badge Registry Numbers
MDL Number MFCD05663876
thermostat Physical Properties
Melting Point 195-199°C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boron-containing reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its application is significant in pharmaceuticals, where it aids in the development of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in materials science for the preparation of advanced polymers and organic electronic materials. Its stability and reactivity make it a valuable tool in research and industrial processes requiring precise and efficient chemical transformations.

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Test Parameter Specification
Appearance White to off-white solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿1,240.00

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N-[4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]methanesulfonamide
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boron-containing reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its application is significant in pharmaceuticals, where it aids in the development of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in materials science for the preparation of advanced polymers

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boron-containing reagent, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Its application is significant in pharmaceuticals, where it aids in the development of drug intermediates and active pharmaceutical ingredients (APIs). Additionally, it is utilized in materials science for the preparation of advanced polymers and organic electronic materials. Its stability and reactivity make it a valuable tool in research and industrial processes requiring precise and efficient chemical transformations.

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