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- Molecular formula
- C10H20S
- CAS Number
- 123-51-3
- IUPAC Name
- 2-methyl-5-(1-methyl-2-sulfanyl-ethyl)cyclohexanethiol
- Molecular Weight
- 188.33g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 0.8590g/cm3
- Synonyms
- Cyclohexaneethanethiol, 3-mercapto-.beta., 4-dimethyl-
Identification
Interesting facts
Interesting Facts about 2-methyl-5-(1-methyl-2-sulfanyl-ethyl)cyclohexanethiol
2-methyl-5-(1-methyl-2-sulfanyl-ethyl)cyclohexanethiol is a fascinating compound with a unique structure and intriguing properties. Here are some noteworthy points to consider:
- Structural Basics: This compound belongs to the class of thiols, which are characterized by the presence of a sulfhydryl group (-SH). This makes it related to alcohols but with sulfur taking the place of oxygen.
- Synthesis Pathways: The synthesis of this compound may involve multi-step reactions typically involving the introduction of the methyl and sulfanyl groups into a cyclohexane ring, showcasing significant synthetic organic chemistry techniques.
- Odor Profile: Similar to many thiols, it is expected to exhibit a strong and often unpleasant odor, which can be reminiscent of rotten vegetables. This property can have implications in both laboratory contexts and practical applications in aroma chemistry.
- Applications: Compounds like this one are often used in research to study thiol reactivity, and some may have relevance in areas such as the development of fragrances or as intermediates in chemical synthesis.
- Biological Relevance: Thiols play significant roles in various biological processes, including enzyme function and redox reactions. Understanding how this compound interacts with biological systems could offer insights into its potential therapeutic applications.
In summary, 2-methyl-5-(1-methyl-2-sulfanyl-ethyl)cyclohexanethiol stands out not only for its chemical structure but also for its wide-ranging implications in both research and practical applications. As scientists continue to explore its properties, new uses may emerge that enhance our understanding of thiolic compounds.