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CAS

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907-04-0

bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 907-04-0 Structure

  • Basic information

    1. Product Name: bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide
    2. Synonyms: bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide
    3. CAS NO:907-04-0
    4. Molecular Formula:
    5. Molecular Weight: 366.541
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 907-04-0.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: bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide(907-04-0)
    11. EPA Substance Registry System: bis-(trans-4-tert-butyl-cyclohexanecarbonyl)-peroxide(907-04-0)

  • 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: 907-04-0(Hazardous Substances Data)

907-04-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 907-04-0 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 9,0 and 7 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 907-04:
(5*9)+(4*0)+(3*7)+(2*0)+(1*4)=70
70 % 10 = 0
So 907-04-0 is a valid CAS Registry Number.

907-04-0Relevant articles and documents

Stereoelectronic Effects in Hydrogen-atom Transfer Reactions of Substituted Cyclohexyl Radicals

Beckwith, Athelstan L. J.,Easton, Christopher J.

, p. 661 - 668 (2007/10/02)

Thermolysis of the peroxyoxalates (1)-(7) and the diacyl peroxides (8)-(11) in cyclohexane at 100 deg C gives cycloalkenes and cycloalkanes by hydrogen-atom transfer reactions of the initially formed conformationally biased 4-t-butyl-, 4-t-butyl-cis,cis-2,6-dimethyl-, 4-t-butyl-cis,trans-2,6-dimethyl-, 4-t-butyl-cis-2-methyl-, 4-t-butyl-trans-2-methyl-, and 5-t-butyl-cis-2-methylcyclohexyl radicals (12)-(17).The composition of the product mixtures indicates that transfer of axial β-hydrogen atoms occurs more rapidly than does transfer of equatorial β-hydrogen atoms.These results support the hypothesis that homolytic fission of a C-H bond is favoured when it lies chlose to the plane of an adjacent semi-occupied orbital.

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