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Atomfair ((2-Phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane C10H11F3OS

Description ((2-Phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane (CAS No. 1640084-14-5) is a high-purity organosulfur compound with the molecular formula C10H11F3OS . This specialty chemical features a trifluoromethylsulfanyloxy group bonded to a 2-phenylpropan-2-yl scaffold, offering unique reactivity for advanced synthetic applications. With a purity of 95%, this compound is ideal for pharmaceutical intermediates, agrochemical research, and materials science. Its IUPAC name is 2-(trifluoromethylsulfanyloxy)propan-2-ylbenzene , and it is supplied as a stable liquid under standard conditions. Proper storage in a cool, dry place with inert atmosphere is recommended to maintain optimal stability.

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Description

Description

((2-Phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane (CAS No. 1640084-14-5) is a high-purity organosulfur compound with the molecular formula C10H11F3OS. This specialty chemical features a trifluoromethylsulfanyloxy group bonded to a 2-phenylpropan-2-yl scaffold, offering unique reactivity for advanced synthetic applications. With a purity of 95%, this compound is ideal for pharmaceutical intermediates, agrochemical research, and materials science. Its IUPAC name is 2-(trifluoromethylsulfanyloxy)propan-2-ylbenzene, and it is supplied as a stable liquid under standard conditions. Proper storage in a cool, dry place with inert atmosphere is recommended to maintain optimal stability.

  • CAS No: 1640084-14-5
  • Molecular Formula: C10H11F3OS
  • Molecular Weight: 236.26
  • Exact Mass: 236.04827063
  • Monoisotopic Mass: 236.04827063
  • IUPAC Name: 2-(trifluoromethylsulfanyloxy)propan-2-ylbenzene
  • SMILES: CC(C)(C1=CC=CC=C1)OSC(F)(F)F
  • Synonyms: 1640084-14-5, ((2-Phenylpropan-2-yl)oxy)(trifluoromethyl)sulfane, (2-Phenylpropan-2-yloxy)(trifluoromethyl)sulfane, (2-Phenylpropan-2-yloxy)(trifluoromethyl)thioether, 95%, 2-(trifluoromethylsulfanyloxy)propan-2-ylbenzene

Application

This compound serves as a versatile building block in medicinal chemistry for introducing trifluoromethylthioether motifs. Researchers utilize it in the development of bioactive molecules due to its ability to modulate lipophilicity and metabolic stability. It is also employed in catalytic transformations and as a precursor for functionalized materials with tailored electronic properties.

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