structure of S-(iodomethyl) ethanethioate

S-(iodomethyl) ethanethioate

CAS No.: 114254-42-1
M. Wt: 216.04
M. Fa: C3H5IOS
InChI Key: -

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

Pictograms

Signal Word

Danger

Safety Data Sheet

Supports customized editing of SDS information and downloading in PDF documents.

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.