| Weight | 116.16 g/mol |
|---|---|
| Formula | C6H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
cis-1,2-Cyclohexanediol (1792-81-0)
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- Azophenolic acerands having chiral 1-phenyl-cis-1,2-cyclohexanediol units : a correlation between enantiorecognitive coloration and host-guest complementarity (Journal of the American Chemical Society, 1993)
- The Role of Neighboring Groups in Replacement Reactions. XXIV.1 The Acetoxy Group. Preparation and Reactions of the Ketene Acetal of cis-1,2-Cyclohexanediol (2-Methylene-cis-4,5-tetramethylenedioxolane)2,3 (Journal of the American Chemical Society, 1958)
- General acid catalyzed acetal hydrolysis. The hydrolysis of acetals and ketals of cis- and trans-1,2-cyclohexanediol. Changes in rate-determining step and mechanism as a function of pH (Journal of the American Chemical Society, 1986)
- Oxidation of trans- and cis-1,2-cyclohexanediol by Gluconobacter oxydans (Applied Microbiology and Biotechnology, 1989)
- Reaction of Some Derivatives of cis-1,2-Cyclohexanediol and cis-1,2-Cyclopentanediol with Anhydrous Hydrogen Fluoride. (Acta Chemica Scandinavica, 1972)
- Notes - A New Synthesis of cis-1,2-Cyclohexanediol (Journal of Organic Chemistry, 1958)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CCC(C(C1)O)O
-
InChIKeyPFURGBBHAOXLIO-UHFFFAOYSA-N
- Pubchem - cis-1,2-Cyclohexanediol
- Wikipedia - cis-cyclohexane-1,2-diol
Cyclohexane-1,2-diol is a chemical compound found in castoreum. It can exist in either cis- or trans-isomers. The enzyme cyclohexane-1,2-diol dehydrogenase uses trans-cyclohexane-1,2-diol and NAD+ to produce 2-hydroxycyclohexan-1-one, NADH and H+.
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