Description

(3-Hydroxy-1-propenyl)sulfur pentafluoride (CAS: 155990-90-2) is a highly specialized organosulfur compound with the molecular formula C₃H₅F₅OS. This technical-grade chemical features a unique pentafluorosulfur group bonded to a 3-hydroxy-1-propenyl moiety, making it a valuable intermediate for advanced synthetic applications. Its high reactivity and fluorine-rich structure lend it utility in pharmaceuticals, agrochemicals, and materials science, particularly in the development of fluorinated polymers and bioactive molecules. The compound is supplied with rigorous quality control to ensure purity and consistency for research and industrial use. Proper handling under inert conditions is recommended due to its potential sensitivity to moisture and air.

Properties

• CAS Number: 155990-90-2
• Complexity: 153
• IUPAC Name: (E)-3-(pentafluoro-lambda6-sulfanyl)prop-2-en-1-ol
• InChI: InChI=1S/C3H5F5OS/c4-10(5,6,7,8)3-1-2-9/h1,3,9H,2H2/b3-1+
• InChI Key: MGHHQQCFLJIKOP-HNQUOIGGSA-N
• Exact Mass: 183.99812676
• Molecular Formula: C3H5F5OS
• Molecular Weight: 184.13
• SMILES: C(/C=C/S(F)(F)(F)(F)F)O
• Topological: 21.2
• Monoisotopic Mass: 183.99812676
• Synonyms: 155990-90-2, (3-Hydroxy-1-propenyl)sulfur pentafluoride, 630-876-5, Pentafluoro(3-hydroxy-1-propenyl)sulfur, (E)-3-(pentafluoro-lambda6-sulfanyl)prop-2-en-1-ol, Sulfur, pentafluoro(3-hydroxy-1-propen-1-yl)-, (OC-6-21)-, Pentafluoro(3-hydroxy-1-propen-1-yl)sulfur, 3-(Pentafluoro-lambda6-sulfanyl)prop-2-en-1-ol, MFCD03789539, SCHEMBL13950535, (3-Hydroxy-1-propenyl)sulfurpentafluoride, CS-0237667, EN300-18634869, (3-Hydroxy-1-propenyl)sulfur pentafluoride, technical grade

(3-Hydroxy-1-propenyl)sulfur pentafluoride serves as a key building block in fluorochemical synthesis, enabling the introduction of sulfur-pentafluoro functional groups into target molecules. Researchers leverage its reactivity to develop novel fluorinated polymers with enhanced thermal and chemical resistance. In pharmaceutical research, it is explored for prodrug design and enzyme inhibition studies due to its electrophilic properties. The compound also finds niche applications in agrochemical optimization for crop protection agents.

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