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93424-16-9

N-benzyl N-propenyl-1 thiobenzamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93424-16-9 Structure

  • Basic information

    1. Product Name: N-benzyl N-propenyl-1 thiobenzamide
    2. Synonyms:
    3. CAS NO:93424-16-9
    4. Molecular Formula:
    5. Molecular Weight: 267.395
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93424-16-9.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: N-benzyl N-propenyl-1 thiobenzamide(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-benzyl N-propenyl-1 thiobenzamide(93424-16-9)
    11. EPA Substance Registry System: N-benzyl N-propenyl-1 thiobenzamide(93424-16-9)

  • 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: 93424-16-9(Hazardous Substances Data)

93424-16-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93424-16-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,4,2 and 4 respectively; the second part has 2 digits, 1 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 93424-16:
(7*9)+(6*3)+(5*4)+(4*2)+(3*4)+(2*1)+(1*6)=129
129 % 10 = 9
So 93424-16-9 is a valid CAS Registry Number.

93424-16-9Downstream Products

93424-16-9Relevant articles and documents

ETUDE COMPARATIVE DE LA PHOTOREACTIVITE D'ENAMIDES ET DE THIOENAMIDS AROMATIQUES TERTIAIRES

Couture, A.,Dubiez, R.,Lablanche-Combier, A.

, p. 1835 - 1844 (2007/10/02)

Photolytic reactions of some simple aromatic enamides and thioenamides illustrate a novel example of the dramatic difference in the photochemical behaviour of carbonyl and thiocarbonyl compounds.In contrast with their oxo-analogues which are photoconverted into enaminoketones, thioenamides undergo photochemical cyclization to yield isoquinolinethione derivatives which can be easily convered into isoquinolones and tetrahydroisoquinolines.

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