S-ethyl azepane-1-carbothioate
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- Molecular formula
- C9H17NS2
- CAS Number
- 10401-56-6
- IUPAC Name
- S-ethyl azepane-1-carbothioate
- Molecular Weight
- 187.33g/mol
- Melting Point
- (Celsius)
- Boiling Point
- (Celsius)
- Density
- 1.0203g/cm3
- Synonyms
- MOLINATE
Identification
Interesting facts
Interesting Facts about S-ethyl azepane-1-carbothioate
S-ethyl azepane-1-carbothioate is a fascinating compound that belongs to the class of thioesters, known for their role in various synthetic and biological processes. Here are some remarkable insights about this compound:
- Structure and Functionality: S-ethyl azepane-1-carbothioate contains a unique seven-membered ring structure (azepane) that contributes to its reactivity and stability. Its thioester functional group (-C(=O)S-) is particularly significant in biochemical processes, such as enzyme catalysis.
- Biological Importance: Compounds like S-ethyl azepane-1-carbothioate can serve as precursors for biologically active molecules. In nature, similar thioesters play crucial roles in cellular metabolism and the biosynthesis of various natural products.
- Synthetic Utility: The compound can act as a versatile building block in organic synthesis. Its ability to participate in nucleophilic acyl substitution reactions makes it valuable for creating complex organic molecules.
- Odor and Flavor Chemistry: Thioesters, including S-ethyl azepane-1-carbothioate, can impart distinct odors and flavors, which find applications in the fragrance and food industries. The unique scent profile of this compound could lead to interesting applications in those fields.
As a Chemistry Student or a Research Scientist, understanding compounds like S-ethyl azepane-1-carbothioate broadens your appreciation of the chemical world and opens doors to innovative research opportunities. Its combination of structural uniqueness and functional versatility exemplifies the intricate interplay of chemistry and biological processes.