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CAS

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24469-13-4

1-(phenylthio)-2-methyl-1-phenyl-1-propene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 24469-13-4 Structure

  • Basic information

    1. Product Name: 1-(phenylthio)-2-methyl-1-phenyl-1-propene
    2. Synonyms: 1-(phenylthio)-2-methyl-1-phenyl-1-propene
    3. CAS NO:24469-13-4
    4. Molecular Formula:
    5. Molecular Weight: 240.369
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 24469-13-4.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-(phenylthio)-2-methyl-1-phenyl-1-propene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-(phenylthio)-2-methyl-1-phenyl-1-propene(24469-13-4)
    11. EPA Substance Registry System: 1-(phenylthio)-2-methyl-1-phenyl-1-propene(24469-13-4)

  • 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: 24469-13-4(Hazardous Substances Data)

24469-13-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24469-13-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,4,6 and 9 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24469-13:
(7*2)+(6*4)+(5*4)+(4*6)+(3*9)+(2*1)+(1*3)=114
114 % 10 = 4
So 24469-13-4 is a valid CAS Registry Number.

24469-13-4Relevant articles and documents

Pd-Catalyzed Alkenyl Thioether Synthesis from Thioesters and N-Tosylhydrazones

Ishitobi, Kota,Muto, Kei,Yamaguchi, Junichiro

, p. 11685 - 11690 (2019/12/02)

A Pd-catalyzed alkenyl thioether synthesis was achieved using thioesters and N-tosylhydrazones as starting materials. The thioester acted as an efficient "sulfur source" for catalytic C-S bond formation using N-tosylhydrazone. This method gave Z-alkenyl thioethers with high diastereoselectivity (up to 99:1 diastereomeric ratio). This transformation displayed a wide functional group tolerance and was successfully applied to the late-stage derivatization of a pharmaceutical molecule to the corresponding alkenyl thioether.

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