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Furan, 2,2,3,3,4,4,5-heptafluorotetrahydro-5-(pentafluoroethyl)-, also known as 2,2,3,3,4,4,5-heptafluorotetrahydrofuran-5-(pentafluoroethyl), is a fluorinated organic compound with the chemical formula C5H3F7O. It is a colorless liquid with a molecular weight of 246.07 g/mol. Furan, 2,2,3,3,4,4,5-heptafluorotetrahydro-5-(pentafluoroethyl)- is characterized by its unique structure, which includes a furan ring with seven fluorine atoms and a pentafluoroethyl group attached to the 5-position. Due to its highly fluorinated nature, it exhibits properties such as high thermal stability, chemical resistance, and low reactivity. These characteristics make it a potential candidate for various applications in the chemical industry, including the synthesis of fluoropolymers, pharmaceuticals, and other specialty chemicals. However, it is important to note that the handling and disposal of such compounds must be done with caution due to their potential environmental and health impacts.

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  • 356-48-9 Structure
  • Basic information

    1. Product Name: Furan, 2,2,3,3,4,4,5-heptafluorotetrahydro-5-(pentafluoroethyl)-
    2. Synonyms:
    3. CAS NO:356-48-9
    4. Molecular Formula: C6F12O
    5. Molecular Weight: 316.046
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 356-48-9.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Furan, 2,2,3,3,4,4,5-heptafluorotetrahydro-5-(pentafluoroethyl)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Furan, 2,2,3,3,4,4,5-heptafluorotetrahydro-5-(pentafluoroethyl)-(356-48-9)
    11. EPA Substance Registry System: Furan, 2,2,3,3,4,4,5-heptafluorotetrahydro-5-(pentafluoroethyl)-(356-48-9)
  • 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: 356-48-9(Hazardous Substances Data)

356-48-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 356-48-9 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,5 and 6 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 356-48:
(5*3)+(4*5)+(3*6)+(2*4)+(1*8)=69
69 % 10 = 9
So 356-48-9 is a valid CAS Registry Number.

356-48-9Downstream Products

356-48-9Relevant articles and documents

Electrochemical fluorination of several esters derived from oxolane-2-yl-carboxylic acid, oxolane-2-yl-methanol and oxane-2-yl-methanol

Abe, Takashi,Tamura, Masanori,Sekiya, Akira

, p. 325 - 332 (2007/10/03)

Electrochemical fluorination (ECF) of the ester derivatives of oxolane-2-yl-carboxylic acid (1), oxolane-2-yl-methanol (2) and oxane-2-yl-methanol (3) were investigated. Perfluoro(oxolane-2-yl- carbonylfluoride) (4) was obtained from derivatives of 1 and 2, and perfluoro(oxane-2-yl-carbonylfluoride) (5) was obtained from derivatives of 3 as the desired compounds, respectively. From the ECF of acetates of 2 and 3, perfluorospiroethers having a dioxolane ring were also obtained as the cyclization product in low yield together with the desired perfluoroacid fluoride (4 and 5). The structure of these perfluorospiroethers was confirmed by analyzing the chlorinated products, which were obtained by the reaction with AlCl3.

Synthesis of Unusual Perfluorocarbon Ethers and Amines Containing Bulky Fluorocarbon Groups: New Biomedical Materials

Huang, Hsu-Nan,Persico, Daniel F.,Lagow, Richard J.,Clark, Leland C.

, p. 78 - 85 (2007/10/02)

The reactions of elemental fluorine with structually crowded hydrocarbon ethers and amines have been studied.The perfluorinated products are currently of interest in biomedical or electronic industrial applications.The syntheses by direct fluorination of perfluoro(tert-butyl methyl ether), perfluoro(tert-butyl isobutyl ether), perfluoro(1,2-di-tert-butoxyethane), perfluoro(cyclohexyl neopentyl ether), perfluoro(2,2,5,5-tetramethyltetrahydrofuran), perfluoro(2,5-dimethyltetrahydrofuran), bis(perfluoroisopropyl) ether, perfluoro(2-ethyltetrahydrofuran), and perfluoro(1,2,2,6,6-pentamethylpiperidine) are reported.The skeletally rearranged byproducts perfluoro(isobutyl methyl ether), perfluoro(2,2,5-trimethyltetrahydrofuran), perfluoro(2,2,5-trimethyltetrahydropyran), 3-hydropentadecafluoro-2,2,5,5-tetramethyltetrahydrofuran, perfluoro(isopropyl propylether), and perfluoro(ethyl isopropyl ether) were also characterized.The 19F and 13C (19F decoupled) NMR assignments of these perfluorinated chemicals are discussed.

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