Atomfair Perfluoroisopropyl iodide C3F7I

Description Perfluoroisopropyl iodide (CAS 677-69-0) is a high-purity fluorinated organic compound with the molecular formula C3F7I and IUPAC name 1,1,1,2,3,3,3-heptafluoro-2-iodopropane . This specialized chemical is characterized by its fully fluorinated isopropyl backbone and reactive iodide moiety, making it a valuable intermediate in advanced synthetic applications. The compound’s exceptional thermal and chemical stability, coupled with its low surface energy, renders it ideal for demanding fluorochemical processes. Available in rigorously controlled batches to ensure consistency, our Perfluoroisopropyl iodide meets the exacting standards of research and industrial applications. Proper handling under inert atmosphere is recommended due to its sensitivity to light and moisture.

Description

Perfluoroisopropyl iodide (CAS 677-69-0) is a high-purity fluorinated organic compound with the molecular formula C₃F₇I and IUPAC name 1,1,1,2,3,3,3-heptafluoro-2-iodopropane. This specialized chemical is characterized by its fully fluorinated isopropyl backbone and reactive iodide moiety, making it a valuable intermediate in advanced synthetic applications. The compound’s exceptional thermal and chemical stability, coupled with its low surface energy, renders it ideal for demanding fluorochemical processes. Available in rigorously controlled batches to ensure consistency, our Perfluoroisopropyl iodide meets the exacting standards of research and industrial applications. Proper handling under inert atmosphere is recommended due to its sensitivity to light and moisture.

CAS No: 677-69-0
Molecular Formula: C3F7I
Molecular Weight: 295.93
Exact Mass: 295.89329
Monoisotopic Mass: 295.89329
IUPAC Name: 1,1,1,2,3,3,3-heptafluoro-2-iodopropane
SMILES: C(C(F)(F)F)(C(F)(F)F)(F)I
Synonyms: Heptafluoroisopropyl iodide, 677-69-0, Perfluoroisopropyl iodide, 1,1,1,2,3,3,3-Heptafluoro-2-iodopropane, Propane, 1,1,1,2,3,3,3-heptafluoro-2-iodo-

Application

Perfluoroisopropyl iodide serves as a key building block in the synthesis of fluorinated polymers and specialty chemicals. It is widely employed in pharmaceutical research for creating radiolabeled compounds and in materials science for developing water- and oil-repellent surfaces. The compound’s unique reactivity also makes it valuable in nucleophilic substitution reactions to introduce perfluoroisopropyl groups into target molecules.

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