Substance
ID:342418
Names and Identifiers
IUPAC Traditional name
3-(hydroxymethyl)phenylboronic acid
IUPAC name
[3-(hydroxymethyl)phenyl]boronic acid
Synonyms
3-Hydroxymethylbenzeneboronic acid3-(Hydroxymethyl)phenylboronic acid3-羟甲基苯硼酸
Properties
Physical Property
Melting Point
95-99 °C(lit.)
Safety Information
MSDS Link
German water hazard class
3
Personal Protective Equipment
Eyeshields, Gloves, type N95 (US), type P1 (EN143) respirator filter
Product Information
Linear Formula
HOCH2C6H4B(OH)2
Molecule Details
Other Notes
Contains varying amounts of anhydride
Packaging
1, 10 g in glass bottle
Application
Reactant involved in:
• Copper-mediated trifluoromethylation1
• Copper-catalyzed transformations from arylboronic acids in water2
• Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate3Reactant involved in the synthesis of biologically active molecules including:
• Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions4
• HIV protease inhibitors with antiviral activity against drug-resistant viruses5
• Pyrrole derivatives for use as PDE4B inhibitors6
Contains varying amounts of anhydride
Packaging
1, 10 g in glass bottle
Application
Reactant involved in:
• Copper-mediated trifluoromethylation1
• Copper-catalyzed transformations from arylboronic acids in water2
• Mitsunobu, Suzuki, and amidation reactions with hydroxyphenylamino bromopyrazinecarboxylate3Reactant involved in the synthesis of biologically active molecules including:
• Mycobacterium tuberculosis H37Rv chorismate mutase inhibitors via Suzuki coupling reactions4
• HIV protease inhibitors with antiviral activity against drug-resistant viruses5
• Pyrrole derivatives for use as PDE4B inhibitors6
Molecular Spectra
No Data Available
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References
No Data Available
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