| Weight | 59.861 g/mol |
|---|---|
| Formula | CH5BO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
Methylboronic acid (13061-96-6)
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- Equilibria and reaction mechanism of the complexation of methylboronic acid with polyols (Inorganic Chemistry, 1992)
- Ruthenium-catalyzed CH Silylation of Methylboronic Acid Using a Removable -Directing Modifier on the Boron Atom (Chemistry Letters, 2011)
- The spectroscopic (FTIR, FT-Raman, NMR and UV), first-order hyperpolarizability and HOMO-LUMO analysis of methylboronic acid. (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2012)
- Organoboranes. 39. Convenient procedures for the preparation of methylboronic acid and trimethylboroxin (Organometallics, 1985)
- An 11B NMR study of the kinetics of methylboronic acidmethylboronate interchange in aqueous solution (Inorganica Chimica Acta, 1997)
- Stereoselective synthesis of dibenzoxapine containing tetrasubstituted exocyclic alkenes via cascade methylboronic acid coupling reactions (Tetrahedron Letters, 2008)
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Predict GHS Hazards for Any Chemical in silico.
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SMILESB(C)(O)O
-
InChIKeyKTMKRRPZPWUYKK-UHFFFAOYSA-N
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Methylboronic acid
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