Name: | 4-(METHANESULFONYLAMINO)PHENYLBORONIC ACID |
CAS: | 380430-57-9 |
Synonyms: | BORONIC ACID, B-[4-[(METHYLSULFONYL)AMINO]PHENYL]- ; 4-(DIHYDROXYBORYL)-N-(METHYLSULFONYL)PHENYLAMINE ; 4-[(METHYLSULPHONYL)AMINO]BENZENEBORONIC ACID ; 4-(METHYLSULFONYLAMINO)PHENYLBORONIC ACID ; BORONIC ACID, [4-[(METHYLSULFONYL)AMINO]PHENYL]- ; 4-(METHANESULFONAMIDO)PHENYLBORONIC ACID ; 4-(METHYLSULFONYLAMINO)BENZENEBORONIC ACID ; 4-N-(METHANESULFONAMIDE)PHENYLBORONIC ACID ; (4-(METHYLSULFONAMIDO)PHENYL)BORONIC ACID ; 4-(METHANESULFONYLAMINO)PHENYLBORONIC ACID ; N-4-METHANESULFONAMIDEPHENYLBORONIC ACID |
MDL.: | MFCD02179473 |
H bond acceptor: | 5 |
H bond donor: | 3 |
Smile: | B(c1ccc(cc1)NS(=O)(=O)C)(O)O |
InChi: | InChI=1S/C7H10BNO4S/c1-14(12,13)9-7-4-2-6(3-5-7)8(10)11/h2-5,9-11H,1H3 |
InChiKey: | InChIKey=NDVJJEADFLTFCD-UHFFFAOYSA-N |
Property |
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Boiling Point: | MP: 148-154 DEG C |
Comments: | APPLICATION: REACTANT FOR PREPARATION OF: POTENT AND SELECTIVE INHIBITORS OF IKK-BETA. INHIBITORS FOR TREATMENT OF OSTEOPOROSIS. INHIBITORS OF HUMAN FARNESYL PYROPHOSPHATE SYNTHASE. SUZUKI-TYPE PD(0) COUPLING REACTIONS IN THE SYNTHESIS OF 2-ARYLPURINES AS CDK INHIBITORS WGK: 1 |
Safety information |
4-(METHANESULFONYLAMINO)PHENYLBORONIC ACID
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