73606-13-0

Basic information

• Product Name: 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE
• Synonyms: 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE;2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULPHONYL FLUORIDE;2-Allyloxy-1,1,2,2-tetrafluoroethanesulfonyl;2-[(Prop-2-en-1-yl)oxy]-1,1,2,2-tetrafluoroethanesulphonyl fluoride;2-(Allyloxy)-1,1,2,2-tetrafluoroethanesulphonylfluoride97%
• CAS NO: 73606-13-0
• Molecular Formula: C₅H₅F₅O₃S
• Molecular Weight: 240.15
• Mol File: 73606-13-0.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 112 °C
• Flash Point: 43.7°C
• Appearance: /
• Density: 1.492g/cm³
• Vapor Pressure: 5.32mmHg at 25°C
• Refractive Index: 1.367
• CAS DataBase Reference: 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE(73606-13-0)
• EPA Substance Registry System: 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE(73606-13-0)

Safety Data

• Hazard Codes: Xi
• Statements: 34
• Safety Statements: 26-36/37/39
• RIDADR: 3265
• HazardClass: IRRITANT
• Hazardous Substances Data: 73606-13-0(Hazardous Substances Data)

Usage

General Description

2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is a chemical compound with the molecular formula C4H3F4O3S. It is commonly used as a reagent in organic synthesis and as a precursor in the production of pharmaceuticals and agrochemicals. 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is highly reactive and should be handled with caution, as it can cause skin and eye irritation upon contact. It is also important to note that 2-ALLYLOXY-1,1,2,2-TETRAFLUOROETHANESULFONYL FLUORIDE is a fluorinated compound, which means it has potential environmental and health implications due to its persistence and bioaccumulation in the environment. Therefore, it should be used and disposed of properly to minimize its impact on human health and the environment.

InChI:InChI=1/C5H5F5O3S/c1-2-3-13-4(6,7)5(8,9)14(10,11)12/h2H,1,3H2

Upstream product

• 556-56-9 allyl iodid 
• 81439-24-9 potassium tetrafluoro(2-fluorosulfonyl)-1-ethanolate 
• 106-95-6 allyl bromide 
• 697-18-7 tetrafluoroethane-β-sultone 

Downstream Products

• 1379588-26-7 C₅H₇F₄O₆S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-40-7 C₂₁H₂₁S⁽¹⁺⁾*C₃₅H₃₉F₁₂O₁₂S^(1-) 
• 1415833-37-2 C₁₆H₂₁F₄O₆S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-33-8 C₁₆H₁₉F₄O₇S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-30-5 C₁₆H₂₁F₄O₇S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-27-0 C₅H₇F₄O₅S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1402927-29-0 C₂₁H₂₁S⁽¹⁺⁾*C₂₇H₃₁F₄O₁₀S^(1-) 
• 1402927-27-8 C₁₆H₁₉F₄O₈S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-13-4 C₁₉H₂₇F₄O₈S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-11-2 C₁₆H₂₁F₄O₇S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 
• 1415833-07-6 C₅H₅F₄O₄S^(1-)*C₂₁H₂₁S⁽¹⁺⁾ 

Relevant articles and documents

NEW POLYFLUOROALKOXYSULFONYL FLUORIDES (I)

The reaction of cyclo-CF2-CF2-O-S(O2)- with haloalkanes (RX, X=Cl,Br,I) in the presence of metal fluorides, MF (M=K+,Cs+,Ag+) was studied as a means for preparing novel reactive polyfluoroalkoxysulfonyl fluorides.The following compounds have been prepared and characterized: ROCF2CF2SO2F where R = CF2=CFCH2CH2, SF5CH2CH2, -CH2-, -CH2-CH2-, CH3CH2CH2, BrCH2CH2, CH2=CHCH2, CH2=CHC(O).Infrared, mass and nmr spectra are presented in order to support the assigned structures.