cis-1,2-Dihydrocatechol
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| IUPAC name
3,5-Cyclohexadiene-1,2-diol
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3D model (JSmol)
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| 200913 | |
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PubChem CID
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CompTox Dashboard (EPA)
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| Properties | |
| C6H8O2 | |
| Molar mass | 112.128 g·mol−1 |
| Appearance | white oily solid |
| Melting point | 28 °C (82 °F; 301 K) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references
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cis-1,2-Dihydrocatechol is the organic compound with the formula C6H6(OH)2. Several isomers exist with this formula. It is a colorless solid melting near room temperature. The compound is classified as a 1,3-cyclohexadiene. It arises by the dihydroxylation of benzene catalyzed by toluene dioxygenase. It can also be prepared from catechol using the enzyme cis-1,2-dihydrobenzene-1,2-diol dehydrogenase:
cis-1,2-Dihydrocatechol has been used in the synthesis, sometimes on a commercial scale, of indinavir, indigo, and poly(p-phenylene).