871329-77-0

Basic information

• Product Name: 3-(N-ISOPROPYLSULFAMOYL)PHENYLBORONIC ACID
• Synonyms: 3-(N-ISOPROPYLSULFAMOYL)PHENYLBORONIC ACID;N-ISOPROPYL 3-BORONOBENZENESULFONAMIDE;3-(IsopropylsulfaMoyl)benzeneboronic acid, 95%;{3-[(propan-2-yl)sulfaMoyl]phenyl}boronic acid
• CAS NO: 871329-77-0
• Molecular Formula: C9H14BNO4S
• Molecular Weight: 243.09
• Product Categories: blocks;BoronicAcids;Sulfonamides
• Mol File: 871329-77-0.mol
• Article Data: 0

Chemical Properties

• Boiling Point: 448.9±55.0 °C(Predicted)
• Appearance: /
• Density: 1.31±0.1 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• PKA: 7.36±0.10(Predicted)
• CAS DataBase Reference: 3-(N-ISOPROPYLSULFAMOYL)PHENYLBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(N-ISOPROPYLSULFAMOYL)PHENYLBORONIC ACID(871329-77-0)
• EPA Substance Registry System: 3-(N-ISOPROPYLSULFAMOYL)PHENYLBORONIC ACID(871329-77-0)

Safety Data

• Hazardous Substances Data: 871329-77-0(Hazardous Substances Data)

Usage

General Description

3-(N-Isopropylsulfamoyl)phenylboronic acid is a boronic acid derivative with the chemical formula C12H17BNO4S. It is used as a reagent in organic synthesis and pharmaceutical research, particularly in the development of new drugs and pharmaceuticals. 3-(N-ISOPROPYLSULFAMOYL)PHENYLBORONIC ACID contains a boronic acid group, which is known to have unique reactivity and can form stable complexes with diols and amines. The N-isopropylsulfamoyl group enhances the solubility and stability of the compound, making it a valuable tool for the synthesis of complex molecules. Its versatile reactivity and strong binding properties make 3-(N-isopropylsulfamoyl)phenylboronic acid a valuable tool for researchers in various fields of chemistry and biomedicine.