3-(Methylsulfonylamino)phenylboronic Acid

≥97%

Reagent Code: #90256
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CAS Number 148355-75-3

science Other reagents with same CAS 148355-75-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.03 g/mol
Formula C₇H₁₀NO₄SB
badge Registry Numbers
MDL Number MFCD02179478
inventory_2 Storage & Handling
Storage 2-8°C

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 significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of bioactive compounds targeting diseases such as cancer, inflammation, and infections. Its boronic acid group makes it valuable in sensor technologies for detecting sugars and other analytes. Additionally, it is utilized in materials science for creating advanced polymers and coatings with specific functional properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,358.00
inventory 5g
10-20 days ฿6,786.00

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3-(Methylsulfonylamino)phenylboronic 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 significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of bioactive compounds targeting diseases such as cancer, inflammation, and infections. Its boronic acid group makes it valuable in sensor technologies for

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of enzyme inhibitors and receptor antagonists. It plays a significant role in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in complex organic molecules. This compound is also employed in the preparation of bioactive compounds targeting diseases such as cancer, inflammation, and infections. Its boronic acid group makes it valuable in sensor technologies for detecting sugars and other analytes. Additionally, it is utilized in materials science for creating advanced polymers and coatings with specific functional properties.

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