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CAS

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74693-95-1

Perfluoro-1-isopropylcyclohexene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74693-95-1 Structure

  • Basic information

    1. Product Name: Perfluoro-1-isopropylcyclohexene
    2. Synonyms: Perfluoro-1-isopropylcyclohexene
    3. CAS NO:74693-95-1
    4. Molecular Formula:
    5. Molecular Weight: 412.073
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74693-95-1.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: Perfluoro-1-isopropylcyclohexene(CAS DataBase Reference)
    10. NIST Chemistry Reference: Perfluoro-1-isopropylcyclohexene(74693-95-1)
    11. EPA Substance Registry System: Perfluoro-1-isopropylcyclohexene(74693-95-1)

  • 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: 74693-95-1(Hazardous Substances Data)

74693-95-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74693-95-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,6,9 and 3 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 74693-95:
(7*7)+(6*4)+(5*6)+(4*9)+(3*3)+(2*9)+(1*5)=171
171 % 10 = 1
So 74693-95-1 is a valid CAS Registry Number.

74693-95-1Downstream Products

74693-95-1Relevant articles and documents

Skeletal transformations and fluorination of perfluoroalkylbenzenes in reactions with antimony pentafluoride

Karpov,Mezhenkova,Platonov

, p. 1176 - 1181 (2007/10/03)

Reaction of octafluorotoluene and perfluoro-m-xylene with tetrafluoroethylene in the presence of SbF5 yielded perfluorinated propyl-and 1,3-dipropylbenzene, and propyltoluene. The perfluoropropyl group of these compounds under the action of SbF5 at 200°C is transformed into perfluoroisopropyl or trifluoromethyl group. Polyfluoroalkylbenzenes in SbF5 medium undergo fluorinationb to afford perfluoro1-alkylcyclohexenes.

Reactions involving Fluoride Ion. Part 18. Derivatives of Perfluorocycloalkenes

Chambers, Richard D.,Taylor, Graham,Powell, Richard L.

, p. 429 - 434 (2007/10/02)

Unlike perfluorocyclobutene, perfluorocyclo-pentene and -hexene do not form oligomers with pyridine.A range of oligomers is obtained from mixtures of perfluorocycloalkenes in reactions initiated by caesium fluoride.Products are also obtained from perfluorocycloalkenes with perfluoropropene and between perfluorocyclobutene and perfluorobut-2-ene.A variation is obseved in the balance between exo- and endo-isomers of perfluorocycloalkene oligomers.It is concluded that conformational interactions dominate the position of equilibrium, exept with four-membered rings, where angle strain is also important.

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