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344564-13-2

2-(1-Phenyl-2-phenylsulfonylaethyl)cyclohexanon is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 344564-13-2 Structure

  • Basic information

    1. Product Name: 2-(1-Phenyl-2-phenylsulfonylaethyl)cyclohexanon
    2. Synonyms:
    3. CAS NO:344564-13-2
    4. Molecular Formula:
    5. Molecular Weight: 342.459
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 344564-13-2.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: 2-(1-Phenyl-2-phenylsulfonylaethyl)cyclohexanon(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(1-Phenyl-2-phenylsulfonylaethyl)cyclohexanon(344564-13-2)
    11. EPA Substance Registry System: 2-(1-Phenyl-2-phenylsulfonylaethyl)cyclohexanon(344564-13-2)

  • 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: 344564-13-2(Hazardous Substances Data)

344564-13-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 344564-13-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,4,4,5,6 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 344564-13:
(8*3)+(7*4)+(6*4)+(5*5)+(4*6)+(3*4)+(2*1)+(1*3)=142
142 % 10 = 2
So 344564-13-2 is a valid CAS Registry Number.

344564-13-2Downstream Products

344564-13-2Relevant articles and documents

NUCLEOPHILIC ADDITION TO STYRYL SULPHONES. PART I. A STUDY ON THE REGIOCHEMISTRY.

Benedetti, F.,Fabrissin, S.,Risaliti, A.

, p. 3887 - 3894 (2007/10/02)

Styryl sulphones undergo nucleophilic addition, with the nucleophile adding at the α- or the β-position, with respect to the sulphone group; β-attack is normally favoured over α-attack.Factors which can change the regioselectivity in favour of the addition of the nucleophile to the α-position are discussed for heteronucleophiles as well as carbon nucleophiles.

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