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CAS

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148601-06-3

1-(benzoylmethyl)-2,2-bis(phenylthio)cyclohexane is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 148601-06-3 Structure

  • Basic information

    1. Product Name: 1-(benzoylmethyl)-2,2-bis(phenylthio)cyclohexane
    2. Synonyms: 1-(benzoylmethyl)-2,2-bis(phenylthio)cyclohexane
    3. CAS NO:148601-06-3
    4. Molecular Formula:
    5. Molecular Weight: 418.624
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 148601-06-3.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: 1-(benzoylmethyl)-2,2-bis(phenylthio)cyclohexane(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(benzoylmethyl)-2,2-bis(phenylthio)cyclohexane(148601-06-3)
    11. EPA Substance Registry System: 1-(benzoylmethyl)-2,2-bis(phenylthio)cyclohexane(148601-06-3)

  • 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: 148601-06-3(Hazardous Substances Data)

148601-06-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 148601-06-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,8,6,0 and 1 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 148601-06:
(8*1)+(7*4)+(6*8)+(5*6)+(4*0)+(3*1)+(2*0)+(1*6)=123
123 % 10 = 3
So 148601-06-3 is a valid CAS Registry Number.

148601-06-3Downstream Products

148601-06-3Relevant articles and documents

Three-Component Radical Condensations Involving Benzoylmethyl Radicals, Alkenes, and Diphenyl Disulfide

Russell, Glen A.,Kulkarni, Shekhar V.

, p. 2678 - 2685 (1993)

Acyl-substituted methyl radicals (RCOCH2.; R = H, Me, Ph), generated by photolysis of RCOCH2HgCl, add to alkenes, enol ethers, or vinyl sulfides to give adduct radicals that are readily trapped by PhSSPh to yield a three-component condensation product.The presence of an alkali metal carbonate is crucial in preventing side reactions resulting in the conversion of the mercurial to RCOCH3 by PhSH formed in the photolysis.

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