| Bioactivity | 1-Phenylethane-1,2-diol is a typical benzyl diol compound. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2-hydroxy-1-phenylethan-1-one) selectively with variety of catalysts, including organocatalysts, metal complexes, non-noble metal oxides, bimetallics[1]. | ||||||||||||
| Name | 1-Phenylethane-1,2-diol | ||||||||||||
| CAS | 93-56-1 | ||||||||||||
| Formula | C8H10O2 | ||||||||||||
| Molar Mass | 138.16 | ||||||||||||
| Transport | Room temperature in continental US; may vary elsewhere. | ||||||||||||
| Storage |
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1-Phenylethane-1,2-diol
CAS: 93-56-1 F: C8H10O2 W: 138.16
1-Phenylethane-1,2-diol is a typical benzyl diol compound. 1-Phenylethane-1,2-diol can be oxidized to hydroxyl ketone (2
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