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CAS

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13127-04-3

trans-1-trifluoromethyl-4-tert-butyl-cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 13127-04-3 Structure

  • Basic information

    1. Product Name: trans-1-trifluoromethyl-4-tert-butyl-cyclohexane
    2. Synonyms: trans-1-trifluoromethyl-4-tert-butyl-cyclohexane
    3. CAS NO:13127-04-3
    4. Molecular Formula:
    5. Molecular Weight: 208.267
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 13127-04-3.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: trans-1-trifluoromethyl-4-tert-butyl-cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: trans-1-trifluoromethyl-4-tert-butyl-cyclohexane(13127-04-3)
    11. EPA Substance Registry System: trans-1-trifluoromethyl-4-tert-butyl-cyclohexane(13127-04-3)

  • 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: 13127-04-3(Hazardous Substances Data)

13127-04-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13127-04-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,2 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 13127-04:
(7*1)+(6*3)+(5*1)+(4*2)+(3*7)+(2*0)+(1*4)=63
63 % 10 = 3
So 13127-04-3 is a valid CAS Registry Number.

13127-04-3Downstream Products

13127-04-3Relevant articles and documents

Convenient synthesis of fluorinated alkanes and cycloalkanes by hydrogenation of perfluoroalkylalkenes under ultrasound irradiation

Carcenac,Tordeux,Wakselman,Diter

, p. 1347 - 1355 (2007/10/03)

Synthesis of several 1,4-disubstituted cyclohexanes, by hydrogenation of sterically hindered and electron poor perfluoroalkyl alkenes, was performed, at room temperature under hydrogen at atmospheric pressure. Hydrogenation was difficult to achieve without ultrasound whatever catalyst and pressure (from 1 to 120 bar) used. Coupling of ultrasonic irradiation with metallic catalysis dramatically increased the efficiency of hydrogenation of perfluoroalkyl alkenes.

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