1,1,2,2-Tetrafluoro-2-(phenylthio)ethanesulfonyl fluoride
CAS No.:
1000294-01-8
M. Wt:
292.24600
M. Fa:
C8H5F5O2S2
InChI Key:
RRIGBESOODESPJ-UHFFFAOYSA-N
Names and Identifiers of 1000294-01-8
CAS Number |
1000294-01-8 |
|---|---|
IUPAC Name |
1,1,2,2-tetrafluoro-2-phenylsulfanylethanesulfonyl fluoride |
InChI |
InChI=1S/C8H5F5O2S2/c9-7(10,8(11,12)17(13,14)15)16-6-4-2-1-3-5-6/h1-5H |
InChIKey |
RRIGBESOODESPJ-UHFFFAOYSA-N |
Canonical SMILES |
C1=CC=C(C=C1)SC(C(F)(F)S(=O)(=O)F)(F)F |
UNSPSC Code |
12352100 |
Physical and chemical properties of 1000294-01-8
Exact Mass |
291.96500 |
|---|---|
LogP |
4.34440 |
Molecular Formula |
C8H5F5O2S2 |
Molecular Weight |
292.24600 |
PSA |
67.82000 |
Safety Information of 1000294-01-8
Applications of 1000294-01-8
The applications of 1,1,2,2-tetrafluoro-2-(phenylthio)ethanesulfonyl fluoride span various fields:
- Organic Synthesis: It serves as a versatile building block in organic synthesis for creating more complex fluorinated compounds.
- Pharmaceutical Development: Its unique properties make it a candidate for drug development, particularly in creating novel therapeutic agents.
- Material Science: The compound's stability and reactivity may find uses in developing advanced materials with specific chemical properties.
Interaction Studies of 1000294-01-8
Studies on the interactions of 1,1,2,2-tetrafluoro-2-(phenylthio)ethanesulfonyl fluoride with biological systems are still emerging. Initial findings suggest it may interact with various biomolecules due to its electrophilic nature. This could lead to modifications in proteins or nucleic acids, influencing biological pathways. Further research is required to elucidate these interactions comprehensively and assess their implications for toxicity and efficacy in biological contexts.
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