| Weight | 116.16 g/mol |
|---|---|
| Formula | C6H12O2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 2 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
1,4-CYCLOHEXANEDIOL
(trans)-isomer of 1,4-cyclohexanediol · (cis)-isomer of 1,4-cyclohexanediol · cis-1,4-cyclohexanediol
931-71-5, 556-48-9, 6995-79-5
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- The Dehydration of 1,4-Cyclohexanediol. Synthesis of 1,4-Epoxycyclohexane1 (Journal of the American Chemical Society, 1944)
- 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)
- Synthesis, Gelation Properties and Photopolymerization of Macrocyclic Diacetylenedicarboxamides Derived from LGlutamic Acid and trans1,4Cyclohexanediol (European Journal of Organic Chemistry, 2011)
- 1,2- and 1,4-Cyclohexanediol: major urinary metabolites and biomarkers of exposure to cyclohexane, cyclohexanone, and cyclohexanol in humans. (International Archives of Occupational and Environmental Health, 1998)
- The mechanism of the loss of H2 and H2O from 1,4-cyclohexanediol anion and related compounds (Journal of Mass Spectrometry, 1983)
- Hydrogenolysis of alcohols: IV. Dehydration of cis- and trans-1,4-cyclohexanediol over nickel-kieselguhr catalyst: Contribution to the mechanism of ether formation (Journal of Catalysis, 1970)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - (trans)-isomer of 1,4-cyclohexanediol
- (cis)-isomer of 1,4-cyclohexanediol
- cis-1,4-cyclohexanediol
- trans-1,4-cyclohexanediol
-
SMILESC1CC(CCC1O)O
-
InChIKeyVKONPUDBRVKQLM-UHFFFAOYSA-N
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(20601-38-1)
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1,4-CYCLOHEXANEDIOL
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