548769-96-6

Basic information

• Product Name: 4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID
• Synonyms: 4-N-BENZYLSULFAMOYLPHENYLBORONIC ACID;4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID;N-BENZYL 4-BORONOBENZENESULFONAMIDE;4-(N-Benzylsulphonamido)benzeneboronic acid 95%;4-(BenzylsulfaMoyl)benzeneboronic acid, 95%;Boronic acid, [4-[[(phenylMethyl)aMino]sulfonyl]phenyl]-;4-(N-Benzylsulphonamido)benzeneboronicacid95%
• CAS NO: 548769-96-6
• Molecular Formula: C₁₃H₁₄BNO₄S
• Molecular Weight: 291.13
• Product Categories: blocks;BoronicAcids;Sulfonamides
• Mol File: 548769-96-6.mol
• Article Data: 2

Chemical Properties

• Melting Point: 148-150
• Boiling Point: 520.535 °C at 760 mmHg
• Flash Point: 268.61 °C
• Appearance: /
• Density: 1.382 g/cm³
• Vapor Pressure: 0mmHg at 25°C
• Refractive Index: 1.632
• Storage Temp.: Keep Cold
• CAS DataBase Reference: 4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID(CAS DataBase Reference)
• NIST Chemistry Reference: 4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID(548769-96-6)
• EPA Substance Registry System: 4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID(548769-96-6)

Safety Data

• Hazard Codes: Xi
• Hazardous Substances Data: 548769-96-6(Hazardous Substances Data)

Usage

General Description

4-(N-benzylsulphonamido)benzeneboronic acid is a chemical compound with the molecular formula C14H15BNO4S. It belongs to the category of boronic acids and derivatives and is used in the synthesis of pharmaceuticals and chemicals. 4-(N-BENZYLSULPHONAMIDO)BENZENEBORONIC ACID is also used in the development of chemical reactions and as a reagent in organic synthesis. It is a white to off-white powder and has the potential to inhibit the activity of certain enzymes. Additionally, it has been studied for its potential therapeutic effects in cancer treatment. Overall, 4-(N-benzylsulphonamido)benzeneboronic acid is a versatile and important compound in the field of organic chemistry and pharmaceutical research.

InChI:InChI=1/C13H14BNO4S/c16-14(17)12-6-8-13(9-7-12)20(18,19)15-10-11-4-2-1-3-5-11/h1-9,15-17H,10H2

Upstream product

• 100-46-9 benzylamine 

Downstream Products

• 1451094-42-0 [4-(4-benzylsulfamoyl-phenyl)-6-fluoro-3-methyl-naphthalen-2-yl]-acetic acid methyl ester 
• 1451094-16-8 [4-(4-benzylsulfamoyl-phenyl)-6-chloro-3-methyl-naphthalen-2-yl]-acetic acid methyl ester 
• 548769-95-5 methyl-phenyl-carbamic acid 4'-benzylsulfamoyl-biphenyl-4-yl ester 

Relevant articles and documents

HALO SULFONYL ARYL BORONATES

The present invention relates to halo sulfonyl aryl boronates of the general formula (I): wherein Arylene designates a carbocyclic or heterocyclic, aromatic ring system comprising 1-3 rings; R1, R2 and R3 are, independently, hydrogen, C1-6alkyl, C1-6alkoxy, halogen, nitro, cyano or phenyl;X is fluoro, chloro or bromo; and Y is a boroxine moiety attached via a bond from Arylene to one of the boron atoms of a boroxine ring which ring has a group of the formula -Arylene(R1)(R2)(R3)SO2X, wherein Arylene, R1, R2, R3 and X are as defined above, at each of the other two boron atoms of the boroxine ring, or Y is a boronic acid group or a boronic ester group.The invention also relates to the preparation of the compounds of formula (I) and to their use in organic synthesis.