512338
4-(Hydroxymethyl)phenylboronic acid
≥95%
Synonym(s):
α-Hydroxy-p-tolueneboronic acid, 4-Hydroxymethylbenzeneboronic acid
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About This Item
Linear Formula:
HOCH2C6H4B(OH)2
CAS Number:
Molecular Weight:
151.96
MDL number:
UNSPSC Code:
12352103
PubChem Substance ID:
NACRES:
NA.22
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Assay
≥95%
mp
251-256 °C (lit.)
functional group
hydroxyl
SMILES string
OCc1ccc(cc1)B(O)O
InChI
1S/C7H9BO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,9-11H,5H2
InChI key
PZRPBPMLSSNFOM-UHFFFAOYSA-N
Application
Reactant involved in the synthesis of biologically active compounds including:
Reactant involved in:
Involved in the synthesis of polyurethane containing spindle-type chromophores
- 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
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Tetrahedron Asymmetry, 14, 3435-3446 (2003)
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