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CAS

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159384-15-3

2-[3,3,4,4-Tetrafluoro-2-(2-hydroxy-ethylsulfanyl)-cyclobut-1-enylsulfanyl]-ethanol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 159384-15-3 Structure

  • Basic information

    1. Product Name: 2-[3,3,4,4-Tetrafluoro-2-(2-hydroxy-ethylsulfanyl)-cyclobut-1-enylsulfanyl]-ethanol
    2. Synonyms: 2-[3,3,4,4-Tetrafluoro-2-(2-hydroxy-ethylsulfanyl)-cyclobut-1-enylsulfanyl]-ethanol
    3. CAS NO:159384-15-3
    4. Molecular Formula:
    5. Molecular Weight: 278.292
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 159384-15-3.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: 2-[3,3,4,4-Tetrafluoro-2-(2-hydroxy-ethylsulfanyl)-cyclobut-1-enylsulfanyl]-ethanol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[3,3,4,4-Tetrafluoro-2-(2-hydroxy-ethylsulfanyl)-cyclobut-1-enylsulfanyl]-ethanol(159384-15-3)
    11. EPA Substance Registry System: 2-[3,3,4,4-Tetrafluoro-2-(2-hydroxy-ethylsulfanyl)-cyclobut-1-enylsulfanyl]-ethanol(159384-15-3)

  • 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: 159384-15-3(Hazardous Substances Data)

159384-15-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 159384-15-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,9,3,8 and 4 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 159384-15:
(8*1)+(7*5)+(6*9)+(5*3)+(4*8)+(3*4)+(2*1)+(1*5)=163
163 % 10 = 3
So 159384-15-3 is a valid CAS Registry Number.

159384-15-3Downstream Products

159384-15-3Relevant articles and documents

Reactions of 1,2-dichlorotetrafluorocyclobut-1-ene and 1,2-dichlorohexafluorocyclopent-1-ene with 2-mercaptoethanol and ethanedithiol and of their products

Mir, Qui-Chee,Shreeve, Jean'ne M.

, p. 269 - 276 (1994)

1,2-Dichlorohexafluorocyclopent-1-ene and 1,2-dichlorotetrafluorocyclobut-1-ene in tetrahydrofuran solutions of 2-mercaptoethanol or 1,2-ethanedithiol and triethylamine give new mono- or di-substituted cycloolefins by displacement of one or two of the chlorine atoms at the double bond by -SCH2CH2OH or -SCH2CH2SH groups, respectively, as a function of the stoichiometry of the reactions.In several cases, the formation of spirocyclic compounds result via an intramolecular cyclization process with concomitant double-bond shift and loss of fluoride ion.Reactions of the spirocycles with nucleophiles, such as N-methylpiperazine, perfluoroglutaryl fluoride and phenylphosphonotionic chloride give rise to more highly substituted olefins and new macrofluoroheterocycles.

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