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CAS 565-48-0

:

cis-4-Hydroxy-α,α,4-trimethylcyclohexanemethanol

Description:
Cis-4-Hydroxy-α,α,4-trimethylcyclohexanemethanol, with the CAS number 565-48-0, is an organic compound characterized by its cyclohexane structure, which features multiple methyl groups and a hydroxyl functional group. This compound is a stereoisomer, specifically the cis form, indicating that the hydroxyl group and the substituents are on the same side of the cyclohexane ring. It is typically a colorless to pale yellow liquid with a characteristic odor. The presence of the hydroxyl group makes it a secondary alcohol, which can participate in hydrogen bonding, influencing its solubility in polar solvents. The trimethyl groups contribute to its hydrophobic character, affecting its physical properties such as boiling point and viscosity. This compound is of interest in various chemical applications, including as a potential intermediate in organic synthesis and in the formulation of fragrances or flavoring agents due to its pleasant aroma. Its stability and reactivity can be influenced by the steric hindrance provided by the bulky methyl groups.
Formula:C10H20O2
InChI:InChI=1/C10H20O2/c1-9(2,11)8-4-6-10(3,12)7-5-8/h8,11-12H,4-7H2,1-3H3/t8-,10+
InChI key:InChIKey=RBNWAMSGVWEHFP-WAAGHKOSNA-N
SMILES:C(C)(C)(O)[C@H]1CC[C@@](C)(O)CC1
Synonyms:
  • 4-(2-Hydroxypropan-2-Yl)-1-Methylcyclohexanol
  • Cyclohexanemethanol, 4-hydroxy-α,α,4-trimethyl-, cis-
  • cis-1,8-p-Menthanediol
  • cis-4-Hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol
  • cis-p-Menthan-1,8-diol
  • p-Menthane-1,8-diol, stereoisomer
  • cis-4-Hydroxy-α,α,4-trimethylcyclohexanemethanol
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