Weight | 184.238 g/mol |
---|---|
Formula | C13H12O |
Hydrogen Acceptors | 1 |
Hydrogen Donors | 1 |
Aromatic Rings | 2 |
Rotatable Bonds | 2 |
Diphenylmethanol (91-01-0)
benzhydrol · benzohydrol · dicyclohexylmethanol
Score:
#276 in Materials science
,
#1815 in Physics
,
#5650 in Chemistry
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- Mechanisms of Photoreactions in Solutions. I. Reduction of Benzophenone by Benzhydrol (Journal of the American Chemical Society, 1961)
- Synthesis and Characterization of New Soluble Polyimides from 3,3,4,4-Benzhydrol Tetracarboxylic Dianhydride and Various Diamines (Chemistry of Materials, 1998)
- Photoinduced reverse atom transfer radical polymerization of methyl methacrylate using camphorquinone/benzhydrol system (Polymer International, 2014)
- Glycosylated derivatives of benzophenone, benzhydrol, and benzhydril as potential venous antithrombotic agents. (Journal of Medicinal Chemistry, 1993)
- Studies in detoxication. 74. The metabolism of benzhydrol, benzophenone and p-hydroxybenzophenone (Biochemical Journal, 1958)
- The Mechanisms of Permanganate Oxidation. III. The Oxidation of Benzhydrol (Journal of the American Chemical Society, 1957)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - benzhydrol
- benzohydrol
- dicyclohexylmethanol
-
SMILESC1=CC=C(C=C1)C(C2=CC=CC=C2)O
-
InChIKeyQILSFLSDHQAZET-UHFFFAOYSA-N
- Pubchem - Diphenylmethanol
- Wikipedia - benzohydrol
Diphenylmethanol, (C6H5)2CHOH (also known as benzhydrol), is a secondary alcohol with a relative molecular mass of 184.23 g/mol. It has a melting point of 69C and a boiling point of 298C. It has uses in perfume and pharmaceutical manufacture.
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