S-(iodomethyl) ethanethioate
Names and Identifiers of S-(iodomethyl) ethanethioate
CAS Number |
114254-42-1 |
|---|---|
IUPAC Name |
S-(iodanylmethyl) ethanethioate |
Canonical SMILES |
CC(=O)SCI |
Physical and chemical properties of S-(iodomethyl) ethanethioate
Molecular Formula |
C3H5IOS |
|---|---|
Molecular Weight |
216.04 |
Safety Information of S-(iodomethyl) ethanethioate
Applications of S-(iodomethyl) ethanethioate
S-(Iodomethyl) ethanethioate has several applications:
- Organic Synthesis: It serves as a versatile building block in organic synthesis, particularly in the formation of more complex sulfur-containing compounds.
- Medicinal Chemistry: Its reactivity makes it useful for modifying biological molecules, which can lead to the development of new pharmaceuticals.
- Chemical Probes: The compound can act as a chemical probe to study biological processes involving thiols and other nucleophiles.
Interaction Studies of S-(iodomethyl) ethanethioate
Interaction studies involving S-(Iodomethyl) ethanethioate focus on its electrophilic nature and how it interacts with various biological targets. These studies often employ techniques like mass spectrometry and nuclear magnetic resonance spectroscopy to elucidate the mechanisms by which this compound modifies proteins or nucleic acids.
Biological Activity of S-(iodomethyl) ethanethioate
Research on S-(Iodomethyl) ethanethioate indicates potential biological activities, particularly as a reactive electrophile that can modify biomolecules. Its ability to alkylate nucleophiles makes it a candidate for studying interactions with proteins and nucleic acids. Such modifications can be useful in understanding mechanisms of action in drug design and development.
