5-Diethylsulfamoyl-2-methylbenzeneboronic acid

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Reagent Code: #90875
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CAS Number 871329-80-5

science Other reagents with same CAS 871329-80-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 271.14 g/mol
Formula C₁₁H₁₈BNO₄S
badge Registry Numbers
MDL Number MFCD08056356
thermostat Physical Properties
Melting Point 146-152°C
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also utilized in the preparation of boron-containing compounds for cancer research and drug discovery. Its boronic acid group makes it valuable in the design of proteasome inhibitors and other therapeutic agents targeting specific biological pathways. Additionally, it is employed in the production of advanced materials and ligands for catalysis in organic chemistry.

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inventory 1g
10-20 days ฿10,000.00

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5-Diethylsulfamoyl-2-methylbenzeneboronic acid
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Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also utilized in the preparation of boron-containing compounds for cancer research and drug discovery. Its boronic acid group makes it valuable in the design of proteasome inhibitors and other ther

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a crucial role in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in complex organic molecules. This compound is also utilized in the preparation of boron-containing compounds for cancer research and drug discovery. Its boronic acid group makes it valuable in the design of proteasome inhibitors and other therapeutic agents targeting specific biological pathways. Additionally, it is employed in the production of advanced materials and ligands for catalysis in organic chemistry.

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