2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl fluoride

Base Information

• Chemical Name: 2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl fluoride
• CAS No.: 73606-13-0
• Molecular Formula: C5H5 F5 O3 S
• Molecular Weight: 240.15
• Hs Code.: 2909199090
• European Community (EC) Number: 671-609-2
• DSSTox Substance ID: DTXSID40381986
• Wikidata: Q81985885
• Mol file: 73606-13-0.mol

Synonyms:73606-13-0;2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl fluoride;1,1,2,2-tetrafluoro-2-prop-2-enoxyethanesulfonyl fluoride;2-allyloxy-1,1,2,2-tetrafluoroethanesulfonylfluoride;2-Allyloxyperfluoroethanesulfonyl fluoride;2-(allyloxy)-1,1,2,2-tetrafluoroethanesulphonyl fluoride;C5H5F5O3S;SCHEMBL2803263;DTXSID40381986;IMNCTHAFGYFIOE-UHFFFAOYSA-N;MFCD03095419;AKOS015839094;CS-0455286;FT-0676776;A837872;2-(allyloxy)-1,1,2,2-tetrafluoroethanesulfonyl fluoride;2-allyloxy-1,1,2,2-tetrafluoro-ethanesulfonyl fluoride;2-(Allyloxy)-1,1,2,2-tetrafluoroethane-1-sulfonyl fluoride;1,1,2,2-tetrafluoro-2-(prop-2-en-1-yloxy)ethane-1-sulfonyl fluoride

Chemical Property of 2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl fluoride

Chemical Property:

• Vapor Pressure: 5.32mmHg at 25°C
• Boiling Point: 112 °C
• Flash Point: 43.7°C
• PSA: 51.75000
• Density: 1.492g/cm³
• LogP: 2.75470
• XLogP3: 2.2
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 8
• Rotatable Bond Count: 5
• Exact Mass: 239.98795600
• Heavy Atom Count: 14
• Complexity: 304

Purity/Quality:

97% ^*data from raw suppliers

2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonylFluoride ^*data from reagent suppliers

Safty Information:

• Hazard Codes: Xi
• Statements: 34
• Safety Statements: 26-36/37/39

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl fluoride

There total 3 articles about 2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl 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:

tetrafluoroethane-β-sultone (697-18-7) + allyl bromide (106-95-6) → 2-Allyloxy-1,1,2,2-tetrafluoro-ethanesulfonyl fluoride (73606-13-0)

Guidance literature:

With silver fluoride; Yield given. Multistep reaction; 1.) diglyme, -196 deg C, then 1 h at room temp.; 2.) -196 deg C, then 12 h at 30-40 deg C;

DOI:10.1016/S0022-1139(00)81557-2

Reference yield:

potassium tetrafluoro(2-fluorosulfonyl)-1-ethanolate (81439-24-9) + allyl bromide (106-95-6) → 2-Allyloxy-1,1,2,2-tetrafluoro-ethanesulfonyl fluoride (73606-13-0)

Guidance literature:

condensation;

Reference yield:

allyl iodid (556-56-9) + potassium tetrafluoro(2-fluorosulfonyl)-1-ethanolate (81439-24-9) → 2-Allyloxy-1,1,2,2-tetrafluoro-ethanesulfonyl fluoride (73606-13-0)

Guidance literature:

condensation;

upstream raw materials:

tetrafluoroethane-β-sultone

allyl bromide

potassium tetrafluoro(2-fluorosulfonyl)-1-ethanolate

allyl iodid

Downstream raw materials:

C₅H₇F₄O₆S^(1-)*C₂₁H₂₁S⁽¹⁺⁾

C₂₁H₂₁S⁽¹⁺⁾*C₃₅H₃₉F₁₂O₁₂S^(1-)

C₁₆H₂₁F₄O₆S^(1-)*C₂₁H₂₁S⁽¹⁺⁾

C₁₆H₁₉F₄O₇S^(1-)*C₂₁H₂₁S⁽¹⁺⁾

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