Perfluoroheptyl iodide

Base Information

• Chemical Name: Perfluoroheptyl iodide
• CAS No.: 335-58-0
• Molecular Formula: C7F15I
• Molecular Weight: 495.958
• Hs Code.: 2903799090
• European Community (EC) Number: 206-393-7
• UNII: S5CHL3HC6D
• DSSTox Substance ID: DTXSID5059828
• Nikkaji Number: J97.537K
• Wikidata: Q81985250
• Mol file: 335-58-0.mol

Synonyms:Perfluoroheptyl iodide;335-58-0;Perfluoro-n-heptyl iodide;1-Iodoperfluoroheptane;1-Iodopentadecafluoroheptane;1,1,1,2,2,3,3,4,4,5,5,6,6,7,7-Pentadecafluoro-7-iodoheptane;Heptane, 1,1,1,2,2,3,3,4,4,5,5,6,6,7,7-pentadecafluoro-7-iodo-;Pentadecafluoroheptyl Iodide;Perfluoro-1-iodoheptane;S5CHL3HC6D;EINECS 206-393-7;MFCD00013712;UNII-S5CHL3HC6D;C7F15I;SCHEMBL1829883;1-Iodoperfluoroheptane (tech.);DTXSID5059828;C7-F15-I;AKOS016015260;FT-0607969;P1839;D92164;Pentadecafluoroheptyl Iodide (stabilized with Na2S2O3);1,1,1,2,2,3,3,4,4,5,5,6,6,7,7-Pentadecafluoro-7-iodoheptane #

Chemical Property of Perfluoroheptyl iodide

Chemical Property:

• Vapor Pressure: 8mmHg at 25°C
• Melting Point: -8°C(lit.)
• Refractive Index: 1.329
• Boiling Point: 139.5 °C at 760 mmHg
• Flash Point: 57.1 °C
• PSA: 0.00000
• Density: 2.024 g/cm³
• LogP: 5.75300
• Storage Temp.: Refrigerator
• Sensitive.: Light Sensitive
• Solubility.: Chloroform (Slightly), Dichloromethane (Slightly), Ethyl Acetate (Very Slightly)
• XLogP3: 6.1
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 15
• Rotatable Bond Count: 5
• Exact Mass: 495.88052
• Heavy Atom Count: 23
• Complexity: 445

Purity/Quality:

98% ^*data from raw suppliers

Perfluoroheptyl Iodide ^*data from reagent suppliers

Safty Information:

• Pictogram(s): Xi
• Hazard Codes: Xi
• Statements: 36/37/38
• Safety Statements: 26-36

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C(C(C(C(F)(F)F)(F)F)(F)F)(C(C(C(F)(F)I)(F)F)(F)F)(F)F
• Uses: Perfluoroheptyl Iodide, is the starting material in the synthesis of Potassium Perfluoroheptanesulfonate (P698195). It is also a Polyfluorinated iodine alkanes (PFIs) derivative, which has shown to have potential estrogenic effects.

Technology Process of Perfluoroheptyl iodide

There total 4 articles about Perfluoroheptyl iodide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

→ perfluoroheptyl iodide (335-58-0)

Guidance literature:

Reference yield:

polytetrafluoroethylene (116-14-3,82785-14-6) + iodotrifluoromethane (2314-97-8,263005-66-9) → Pentafluoroethyl iodide (354-64-3) + 1,1,1,2,2,3,3-heptafluoro-3-iodo-propane (754-34-7) + 1-iodo-2,2,3,3,4,4,5,5,5-nonafluorobutane (423-39-2) + undecafluoro-1-iodopentane (638-79-9) + n-perfluorohexyl iodide (355-43-1) + perfluoroheptyl iodide (335-58-0)

Guidance literature:

In gas; Product distribution; Quantum yield; Thermodynamic data; Irradiation; pulsed CO₂ laser; release of reaction enthalpy, selectivity depending on pressure and temperature;

DOI:10.1021/j100379a034

Reference yield:

→ perfluoroheptyl iodide (335-58-0)

Guidance literature:

With iodine;

DOI:10.1039/jr9520004259

upstream raw materials:

polytetrafluoroethylene

iodotrifluoromethane

Downstream raw materials:

pentadecafluoroheptylbenzene

Perfluorooctanoic acid

1-phenylperfluorononyne

1-(Perfluorheptyl)-2-phenylaethen

Refernces

• 1、 -. "Perfluoroalkyl compounds and process for preparing the same". . . Retrieved 2008/06/13.