Perfluorohexanesulphonyl fluoride

Base Information

• Chemical Name: Perfluorohexanesulphonyl fluoride
• CAS No.: 423-50-7
• Molecular Formula: C6F14O2S
• Molecular Weight: 402.108
• Hs Code.: 2904909090
• European Community (EC) Number: 207-026-3
• DSSTox Substance ID: DTXSID3059973
• Nikkaji Number: J26.737F
• Wikidata: Q72500656
• Mol file: 423-50-7.mol

Synonyms:423-50-7;perfluorohexanesulfonyl fluoride;Perfluorohexanesulphonyl fluoride;Perflurohexane sulphonyl fluoride;PERFLUOROHEXANE SULPHONYL FLUORIDE;1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluorohexane-1-sulfonyl fluoride;C6F14O2S;1,1,2,2,3,3,4,4,5,5,6,6,6-Tridecafluoro-1-hexanesulfonyl fluoride;tridecafluorohexane-1-sulfonyl fluoride;EINECS 207-026-3;1-Hexanesulfonyl fluoride, 1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluoro-;Perfluorohexylsulfonyl fluoride;C6F13SO2F;SCHEMBL584177;perfluorohexyl sulfonyl fluoride;perfluorohexane sulfonyl fluoride;DTXSID3059973;Perfluorhexane sulphonyl fluoride;C6-F14-O2-S;CS-B0906;MFCD00042452;AKOS025311009;AS-15242;FT-0632118;EN300-736040;W-109534

Chemical Property of Perfluorohexanesulphonyl fluoride

Chemical Property:

• Vapor Pressure: 25.5mmHg at 25°C
• Refractive Index: 1.286
• Boiling Point: 112.6 °C at 760 mmHg
• Flash Point: 21.9 °C
• PSA: 42.52000
• Density: 1.785 g/cm³
• LogP: 5.06280
• XLogP3: 4.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 16
• Rotatable Bond Count: 5
• Exact Mass: 401.9395447
• Heavy Atom Count: 23
• Complexity: 551

Purity/Quality:

98% ^*data from raw suppliers

PerfluorohexaneSulphonylFluoride ^*data from reagent suppliers

Safty Information:

• Pictogram(s): C
• Hazard Codes: C
• Statements: 20/21/22-34
• Safety Statements: 26-36/37/39

MSDS Files:

Useful:

• Canonical SMILES: C(C(C(C(F)(F)S(=O)(=O)F)(F)F)(F)F)(C(C(F)(F)F)(F)F)(F)F

Technology Process of Perfluorohexanesulphonyl fluoride

There total 5 articles about Perfluorohexanesulphonyl fluoride 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:

1-hexanesulfonyl chloride (14532-24-2) → tridecafluorohexanesulfonyl fluoride (423-50-7)

Guidance literature:

With hydrogen fluoride; anodische Fluorierung;

DOI:10.1039/jr9570002640

Reference yield:

Hexamethylene sulfone (6251-33-8) → tridecafluorohexanesulfonyl fluoride (423-50-7)

Guidance literature:

With hydrogen fluoride; Electrochem. Process; electrofluorination;

Reference yield:

2,2,3,3,4,4,5,5,6,6,6-undecafluoro-hexanesulfonyl fluoride → tridecafluorohexanesulfonyl fluoride (423-50-7)

Guidance literature:

With 1,1,2-Trichloro-1,2,2-trifluoroethane; fluorine; for 0.6h;

DOI:10.1016/j.jfluchem.2004.09.024

upstream raw materials:

1-hexanesulfonyl chloride

2,2,3,3,4,4,5,5,6,6,6-undecafluoro-hexanesulfonyl chloride

hydrogen fluoride

Hexamethylene sulfone

Downstream raw materials:

perfluorohexane-1-sulfonic acid

tridecafluorohexane-1-sulfonic acid potassium salt

1,1,2,2,3,3,4,4,5,5,6,6,6-tridecafluoro-n-hexane-1-sulfonamide

heptadecafluoro-octane-1-sulfonic acid amide

Refernces