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CAS 1845-59-6

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(1S,2S,5S)-2-Methyl-5-(1-methylethyl)cyclohexanol

Description:
(1S,2S,5S)-2-Methyl-5-(1-methylethyl)cyclohexanol, with the CAS number 1845-59-6, is a chiral alcohol characterized by its cyclohexane ring structure, which is substituted with a methyl group and an isopropyl group. This compound exhibits stereochemistry at three specific carbon centers, contributing to its unique spatial arrangement and potential optical activity. As a secondary alcohol, it features a hydroxyl (-OH) group attached to a carbon that is also bonded to two other carbon atoms. The presence of bulky substituents, such as the isopropyl group, can influence its physical properties, including boiling point and solubility. Typically, such compounds may exhibit moderate polarity due to the hydroxyl group, making them soluble in polar solvents while being less soluble in non-polar solvents. Additionally, the stereochemistry can affect the compound's reactivity and interactions in biological systems, potentially influencing its applications in pharmaceuticals or as a chiral building block in organic synthesis.
Formula:C10H20O
InChI:InChI=1S/C10H20O/c1-7(2)9-5-4-8(3)10(11)6-9/h7-11H,4-6H2,1-3H3/t8-,9-,10-/m0/s1
InChI key:InChIKey=ULJXKUJMXIVDOY-GUBZILKMSA-N
SMILES:C(C)(C)[C@@H]1C[C@H](O)[C@@H](C)CC1
Synonyms:
  • p-Menthan-2-ol, (1S,2S,4S)-(+)-
  • (1S-(1alpha,2beta,5alpha))-5-(Isopropyl)-2-methylcyclohexan-1-ol
  • Cyclohexanol, 2-methyl-5-(1-methylethyl)-, [1S-(1α,2β,5α)]-
  • (+)-Carvomenthol
  • 2-methyl-5-(propan-2-yl)cyclohexanol
  • Cyclohexanol, 2-methyl-5-(1-methylethyl)-, (1S,2S,5S)-
  • (1S,2S,5S)-2-Methyl-5-(1-methylethyl)cyclohexanol
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