Basic Information |
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Product Name: | 4-(HYDROXYMETHYL)PHENYLBORONIC ACID |
CAS: | 59016-93-2 |
English Synonyms: | BORONIC ACID, [4-(HYDROXYMETHYL)PHENYL]- ; 4-(HYDROXYLMETHYL)PHENYLBORONIC ACID ; 4-(HYDROXYMETHYL)PHENYLBORONIC ACID ; P-(HYDROXYMETHYL)PHENYLBORONIC ACID ; [4-(HYDROXYMETHYL)PHENYL]BORANEDIOL ; 4-(HYDROXYMETHYL)BENZENEBORONIC ACID ; ALPHA-HYDROXY-P-TOLUENEBORONIC ACID ; (4-BORONOPHENYL)METHANOL ; 4-BORONOBENZYL ALCOHOL ; (4-(HYDROXYMETHYL)PHENYL)BORONIC ACID |
MDL Number.: | MFCD00792672 |
H bond acceptor: | 3 |
H bond donor: | 3 |
Smile: | B(c1ccc(cc1)CO)(O)O |
InChi: | InChI=1S/C7H9BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,9-11H,5H2 |
InChiKey: | InChIKey=PZRPBPMLSSNFOM-UHFFFAOYSA-N |
Property |
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Melting Point: | 251-256 DEG C(LIT)/251-256 °C |
Comments: | APPLICATION: REACTANT INVOLVED IN THE SYNTHESIS OF BIOLOGICALLY ACTIVE COMPOUNDS INCLUDING: IMIDAZO[4,5-B]PYRAZIN-2-ONES FOR USE AS MTOR KINASE INHIBITORS HUMAN IMMUNODIFICIENCY VIRUS PROTEASE INHIBITORS WITH ACTIVITY AGAINST RESISTANT VIRUSES REACTANT INVOLVED IN: SUZUKI COUPLING REACTIONS, COPPER-CATALYZED TRANSFORMATION FROM ARYLBORONIC ACIDS IN WATER INVOLVED IN THE SYNTHESIS OF POLYURETHANE CONTAINING SPINDLE-TYPE CHROMOPHORES UNSPSC: 12352103 WGK: 3 |
Safety information |
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WGK Germany: | 3 |
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