Weight | 118.176 g/mol |
---|---|
Formula | C6H14O2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 2 |
Aromatic Rings | 0 |
Rotatable Bonds | 1 |
PINACOL (76-09-5)
BM567 · BM 567
Score:
#5856 in Chemistry
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- Synthesis of pinacol arylboronates via cross-coupling reaction of bis(pinacolato)diboron with chloroarenes catalyzed by palladium(0)-tricyclohexylphosphine complexes (Tetrahedron, 2001)
- Strategic Use of Pinacol-Terminated Prins Cyclizations in Target-Oriented Total Synthesis (Journal of Organic Chemistry, 2003)
- Regio- and enantiocontrol in the room-temperature hydroboration of vinyl arenes with pinacol borane. (Journal of the American Chemical Society, 2004)
- Enantioselective Photoredox Catalysis Enabled by Proton-Coupled Electron Transfer: Development of an Asymmetric Aza-Pinacol Cyclization (Journal of the American Chemical Society, 2013)
- An improved system for the palladium-catalyzed borylation of aryl halides with pinacol borane. (Journal of Organic Chemistry, 2008)
- Direct Conversion of Arylamines to Pinacol Boronates: A Metal-Free Borylation Process (Angewandte Chemie, 2010)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - BM567
- BM 567
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SMILESCC(C)(C(C)(C)O)O
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InChIKeyIVDFJHOHABJVEH-UHFFFAOYSA-N
- Pubchem - PINACOL
- Wikipedia - pinacol
Pinacol is a white solid organic compound. It is a diol that has hydroxyl groups (-OH) on vicinal carbon atoms.
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