Interesting facts
              Interesting Facts about 4-(1-Hydroxy-1-methyl-ethyl)-1-methyl-cyclohexanol
4-(1-Hydroxy-1-methyl-ethyl)-1-methyl-cyclohexanol is an intriguing compound with a unique structure, making it a subject of interest in both organic chemistry and the field of natural product synthesis. Here are some captivating insights about this compound:
- Structural Complexity: The presence of both hydroxy and alkyl groups in its structure contributes to its interesting chemical properties. This complexity can lead to diverse reactivity patterns in various chemical reactions.
 - Chirality: The compound is chiral, meaning it can exist in multiple forms (enantiomers). This property is significant in pharmacology, as different enantiomers can exhibit different biological activities.
 - Potential Applications: Compounds with similar structures are often studied for their potential applications in fragrances, flavors, or as intermediates in pharmaceutical synthesis. This compound could potentially serve as a building block for more complex molecules in drug development.
 - Research Significance: As a derivative of cyclohexanol, it can be studied for its role in understanding the conformational behavior of cyclic alcohols. This knowledge is crucial for predicting the behavior of similar compounds in various environments.
 - Natural Occurrence: Compounds with related structures often occur in nature, and their study can lead to the identification of new natural products with therapeutic properties. Research into this compound may reveal connections to biologically active substances occurring in different plants or microorganisms.
 
In the world of organic compounds, 4-(1-hydroxy-1-methyl-ethyl)-1-methyl-cyclohexanol stands as a testament to the intricate relationships between structure and function, sparking curiosity among chemists and students alike. Its unique features serve as an exciting point of exploration in synthetic and medicinal chemistry.
Synonyms
          TERPIN
          p-Menthane-1,8-diol
          trans-Terpin
          80-53-5
          565-48-0
          cis-p-Menthan-1,8-diol
          1,8-Terpin
          4-(2-hydroxypropan-2-yl)-1-methylcyclohexan-1-ol
          565-50-4
          Terpin, trans-
          cis-1,8-p-Menthanediol
          trans-1,8-Terpin
          trans-p-Menthan-1,8-diol
          Terpene
          NSC 403856
          cis-4-Hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol
          Terpin trans-form [MI]
          trans-1,8-p-Menthanediol
          trans-p-Menthane-1,8-diol
          (Z)-terpin
          Terpinol
          NSC-403856
          4HW1S44T5G
          MPF495B08R
          Cyclohexanemethanol, 4-hydroxy-.alpha.,.alpha.,4-trimethyl-
          DTXSID7023643
          4-(2-Hydroxypropan-2-yl)-1-methylcyclohexanol
          NCGC00159414-02
          4-p-Menthan-1,8-diol
          Dipenteneglycol
          Terpin (VAN)
          Terpin [BAN]
          UNII-4HW1S44T5G
          UNII-MPF495B08R
          Terpinhydrat
          trans_terpin
          EINECS 201-288-2
          EINECS 209-279-5
          p-Mentha-1,8-diol
          TERPIN [WHO-DD]
          TERPIN [MI]
          cis-p-Menthane-1,8-diol
          EC 201-288-2
          SCHEMBL19192
          4-Hydroxy-alpha,alpha,4-trimethylcyclohexanemethanol
          DTXCID903643
          SCHEMBL5377815
          SCHEMBL9536260
          CHEMBL1414114
          CHEMBL1513871
          CHEMBL1651998
          Cyclohexanemethanol, 4-hydroxy-alpha,alpha,4-trimethyl-
          CHEBI:134806
          CHEBI:179539
          DTXSID401031800
          DTXSID501031803
          Pharmakon1600-01506188
          Cyclohexanemethanol, 4-hydroxy-alpha,alpha,4-trimethyl-, trans-
          HY-N4324
          Tox21_111646
          BBL034665
          NSC403856
          NSC760418
          STL356461
          AKOS022099020
          AKOS024348939
          AKOS037514988
          CAS-80-53-5
          Cyclohexanemethanol,.alpha.,4-trimethyl-
          NCGC00159414-01
          NCGC00159414-03
          NCGC00159414-04
          NCGC00159414-05
          NCGC00159414-06
          NCGC00166136-01
          AS-83272
          DA-48919
          NCI60_003817
          PD132153
          SID124892172
          trans-Terpin, analytical standard, for GC
          CS-0032749
          NS00004546
          NS00079759
          T2344
          G83071
          SBI-0653368.0001
          AB01563167_01
          4-(1-Hydroxy-1-methylethyl)-1-methylcyclohexanol
          cis-4-Hydroxy-|A,|A,4-trimethylcyclohexanemethanol
          TERPIN MONOHYDRATE IMPURITY D [EP IMPURITY]
          4-(1-Hydroxy-1-methylethyl)-1-methylcyclohexanol #
          BRD-K93396439-002-01-2
          Q27259605
          Q27284154
          (1R,4R)-4-(2-HYDROXYPROPAN-2-YL)-1-METHYLCYCLOHEXAN-1-OL
          CYCLOHEXANEMETHANOL, 4-HYDROXY-.ALPHA.,.ALPHA.,4-TRIMETHYL-, CIS-
          CYCLOHEXANEMETHANOL, 4-HYDROXY-.ALPHA.,.ALPHA.,4-TRIMETHYL-, TRANS-
              
Solubility of 4-(1-hydroxy-1-methyl-ethyl)-1-methyl-cyclohexanol
Understanding the solubility of 4-(1-hydroxy-1-methyl-ethyl)-1-methyl-cyclohexanol can provide valuable insights into its potential applications and behaviors in various environments. Here are some key points to consider:
In conclusion, while 4-(1-hydroxy-1-methyl-ethyl)-1-methyl-cyclohexanol may exhibit reasonable solubility in certain solvents, understanding the balance between its hydrophobic and hydrophilic parts is crucial. As noted, "solubility is the key to reactivity," and this principle applies here as well.