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CAS

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184899-81-8

propane, 1,1,1,2,2,3,3-heptafluoro-3-(fluoromethoxy)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 184899-81-8 Structure

  • Basic information

    1. Product Name: propane, 1,1,1,2,2,3,3-heptafluoro-3-(fluoromethoxy)-
    2. Synonyms: 1,1,1,2,2,3,3-Heptafluoro-3-(fluoromethoxy)propane; Fluoromethyl heptafluoropropyl ether
    3. CAS NO:184899-81-8
    4. Molecular Formula: C4H2F8O
    5. Molecular Weight: 218.0453
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 184899-81-8.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 22.274°C at 760 mmHg
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: 1.507g/cm3
    6. Vapor Pressure: 837.2mmHg at 25°C
    7. Refractive Index: 1.258
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: propane, 1,1,1,2,2,3,3-heptafluoro-3-(fluoromethoxy)-(CAS DataBase Reference)
    11. NIST Chemistry Reference: propane, 1,1,1,2,2,3,3-heptafluoro-3-(fluoromethoxy)-(184899-81-8)
    12. EPA Substance Registry System: propane, 1,1,1,2,2,3,3-heptafluoro-3-(fluoromethoxy)-(184899-81-8)

  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 184899-81-8(Hazardous Substances Data)

184899-81-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 184899-81-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,8,4,8,9 and 9 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 184899-81:
(8*1)+(7*8)+(6*4)+(5*8)+(4*9)+(3*9)+(2*8)+(1*1)=208
208 % 10 = 8
So 184899-81-8 is a valid CAS Registry Number.

184899-81-8Downstream Products

184899-81-8Relevant articles and documents

New synthetic method of alkyl perfluoroalkyl ethers

Tamura, Masanori,Takubo, Seij,Quan, Heng-Dao,Sekiya, Akira

, p. 343 - 344 (2007/10/03)

vic-Difluorination of alkyl perfluoroenol ethers proceeded with high- valence metal fluoride, such as cobalt (III) fluoride and potassium tetrafluorocobaltate, in good yields to afford alkyl perfluoroalkyl ethers.

Technology for the preparation of perfluoro-organic compounds

Moldavskii, Dmitrii D.,Bispen, Tatjana A.,Kaurova, Galina I.,Furin, Georgii G.

, p. 157 - 167 (2007/10/03)

Fluorination by elemental fluorine of fluorine-containing alkenes, alkanes, ethers and tertiary amines was investigated, aimed at obtaining the perfluorinated analogs. The factors affecting yield of the target compounds were studied. Elements of technology were elucidated.

Synthesis of perfluorinated paraffins, esters, and tertiary amines by direct fluorination with elemental fluorine

Bispen,Moldavskii

, p. 1009 - 1013 (2007/10/03)

Fluorination of partially fluorinated olefins, paraffins, ethers, and tertiary amines with elemental fluorine at the gas-liquid interface under various conditions was studied.

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