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115869-06-2

1,1-bis(trifluoroacetoxy)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 115869-06-2 Structure

  • Basic information

    1. Product Name: 1,1-bis(trifluoroacetoxy)cyclohexane
    2. Synonyms: 1,1-bis(trifluoroacetoxy)cyclohexane
    3. CAS NO:115869-06-2
    4. Molecular Formula:
    5. Molecular Weight: 308.177
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 115869-06-2.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: 1,1-bis(trifluoroacetoxy)cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1,1-bis(trifluoroacetoxy)cyclohexane(115869-06-2)
    11. EPA Substance Registry System: 1,1-bis(trifluoroacetoxy)cyclohexane(115869-06-2)

  • 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: 115869-06-2(Hazardous Substances Data)

115869-06-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 115869-06-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,5,8,6 and 9 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 115869-06:
(8*1)+(7*1)+(6*5)+(5*8)+(4*6)+(3*9)+(2*0)+(1*6)=142
142 % 10 = 2
So 115869-06-2 is a valid CAS Registry Number.

115869-06-2Relevant articles and documents

Practical synthesis of gem-difluorides from cyclohexanone: Synthesis of gem-bistrifluoroacetates and their reactions with fluoride nucleophiles

Tojo, Masahiro,Fukuoka, Shinsuke,Tsukube, Hiroshi

experimental part, p. 29 - 35 (2010/03/30)

Formation of ketone acylals bearing trihaloacetoxy groups and their nucleophilic geminal disubstitution by fluoride ions were investigated. Cyclohexanone reacted with trifluoroacetic anhydride without catalyst to give gem-bistrifluoroacetates via a concerted bimolecular reaction. Treatment with hydrogen fluoride under mild conditions efficiently yielded the corresponding gem-difluorides. In this reaction process, trifluoroacetic acid was recovered and converted to trifluoroacetic anhydride using P2O5. Since gem-difluorides were derived from ketones, HF and P2O5, this constitutes a practical synthesis of gem-difluorides.

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