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cis-1,2-Dihydrocatechol

Names
IUPAC name 3,5-Cyclohexadiene-1,2-diol
Identifiers
CAS Number	17793-95-2
3D model (JSmol)	Interactive image
ChEBI	CHEBI:16190
ChemSpider	154113
Gmelin Reference	200913
KEGG	C04091
PubChem CID	176951
CompTox Dashboard (EPA)	DTXSID70880013
InChI InChI=1S/C6H8O2/c7-5-3-1-2-4-6(5)8/h1-8H/t5-,6+Key: YDRSQRPHLBEPTP-OLQVQODUSA-N
SMILES C1=C((C=C1)O)O
Properties
Chemical formula	C6H8O2
Molar mass	112.128 g·mol
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 , 100 kPa). Infobox references

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.

cis-1,2-Dihydrocatechol has been used in the synthesis, sometimes on a commercial scale, of indinavir, indigo, and poly(p-phenylene).

References

1. Hudlicky, Tomas; Thorpe, Andrew J. (1996). "Current Status and Future Perspectives of Cyclohexadiene-cis-diols in Organic Synthesis: Versatile Intermediates in the Concise Design of Natural Products". Chemical Communications (17): 1993. doi:10.1039/cc9960001993.

• Cyclohexadienes
• Conjugated dienes