871329-76-9

Basic information

• Product Name: 3-(N-ETHYLSULFAMOYL)PHENYLBORONIC ACID
• Synonyms: ETHYL 3-BORONOBENZENESULFONAMIDE;3-(N-ETHYLSULFAMOYL)PHENYLBORONIC ACID;3-(EthylsulfaMoyl)benzeneboronic acid, 97%
• CAS NO: 871329-76-9
• Molecular Formula: C₈H₁₂BNO₄S
• Molecular Weight: 229.06
• Product Categories: blocks;BoronicAcids;Sulfonamides
• Mol File: 871329-76-9.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 3-(N-ETHYLSULFAMOYL)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(N-ETHYLSULFAMOYL)PHENYLBORONIC ACID(871329-76-9)
• EPA Substance Registry System: 3-(N-ETHYLSULFAMOYL)PHENYLBORONIC ACID(871329-76-9)

Safety Data

• Hazardous Substances Data: 871329-76-9(Hazardous Substances Data)

Usage

General Description

3-(N-ethylsulfamoyl)phenylboronic acid is a chemical compound with the molecular formula C10H14BNO4S. It is a boronic acid derivative that contains a phenyl ring with an attached sulfamoyl group and an ethyl group. 3-(N-ETHYLSULFAMOYL)PHENYLBORONIC ACID is commonly used in organic synthesis as a reagent for the Suzuki-Miyaura coupling reaction, which is a widely used method for the formation of carbon-carbon bonds. It is also used in the development of pharmaceuticals and agrochemicals due to its boronic acid moiety, which has been found to be an important pharmacophore in many bioactive compounds. Additionally, 3-(N-ethylsulfamoyl)phenylboronic acid has potential applications in the field of materials science, particularly in the development of functional materials and sensors.

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