| Weight | 366.46 g/mol |
|---|---|
| Formula | C26H22O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 4 |
| Rotatable Bonds | 5 |
Benzopinacol (464-72-2)
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LabBot
- Laser-induced crystal growth and morphology control of benzopinacol produced from benzophenone in ethanol/water mixed solution (Crystal Growth & Design, 2004)
- The Pinacol Rearrangement in the Heterocyclic Series. I. Pyridine Analogs of Benzopinacol (Journal of the American Chemical Society, 1953)
- Kinetics and Mechanism of the Pinacol Rearrangement. I. The Perchloric Acid-catalyzed Rearrangement of Benzopinacol and of Tetraphenylethylene Oxide in Acetic Acid Solution1 (Journal of the American Chemical Society, 1954)
- Atomic force microscopy and SolidState rearrangement of benzopinacol (Journal of Physical Organic Chemistry, 1995)
- Anodic Reductions. I. Conversion of Benzophenone to Benzopinacol by Unipositive Magnesium (Journal of the American Chemical Society, 1954)
- Reactions of benzopinacol with group 13 alkyl metals : Crystal structure of Me6In4 [OC (C6H5)2C (C6H5)2O]2 (OCH3 )2, a new alkylalkoxo indium diolate (Polyhedron, 2007)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C(C2=CC=CC=C2)(C(C3=CC=CC=C3)(C4=CC=CC=C4)O)O
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InChIKeyMFEWNFVBWPABCX-UHFFFAOYSA-N
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Benzopinacol
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