871329-73-6 Usage
General Description
5-(N-benzylsulfamoyl)-2-methylphenylboronic acid is a chemical compound that is used as a building block in organic synthesis. It contains a boronic acid group, which is commonly used in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. The presence of the benzylsulfamoyl group makes this compound useful for selective proteolysis and bioconjugation applications, as it can specifically target and modify proteins and peptides. The methylphenyl group provides steric hindrance, which can influence the reactivity and selectivity of the compound in various chemical reactions. Overall, 5-(N-benzylsulfamoyl)-2-methylphenylboronic acid has versatile applications in organic synthesis, bioconjugation, and medicinal chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 871329-73-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,7,1,3,2 and 9 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 871329-73:
(8*8)+(7*7)+(6*1)+(5*3)+(4*2)+(3*9)+(2*7)+(1*3)=186
186 % 10 = 6
So 871329-73-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H16BNO4S/c1-11-7-8-13(9-14(11)15(17)18)21(19,20)16-10-12-5-3-2-4-6-12/h2-9,16-18H,10H2,1H3
