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33414-69-6

Benzenepropanamide, b-oxo-N-phenyl-a-(phenylimino)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 33414-69-6 Structure

  • Basic information

    1. Product Name: Benzenepropanamide, b-oxo-N-phenyl-a-(phenylimino)-
    2. Synonyms:
    3. CAS NO:33414-69-6
    4. Molecular Formula: C21H16N2O2
    5. Molecular Weight: 328.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 33414-69-6.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: Benzenepropanamide, b-oxo-N-phenyl-a-(phenylimino)-(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzenepropanamide, b-oxo-N-phenyl-a-(phenylimino)-(33414-69-6)
    11. EPA Substance Registry System: Benzenepropanamide, b-oxo-N-phenyl-a-(phenylimino)-(33414-69-6)

  • 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: 33414-69-6(Hazardous Substances Data)

33414-69-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 33414-69-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,3,4,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 33414-69:
(7*3)+(6*3)+(5*4)+(4*1)+(3*4)+(2*6)+(1*9)=96
96 % 10 = 6
So 33414-69-6 is a valid CAS Registry Number.

33414-69-6Downstream Products

33414-69-6Relevant articles and documents

Conjugated Schiff's Bases. Part 12. Kinetics and Mechanism of Condensation of Active Methylene Derivatives (CH-Acids) with Nitrosobenzene

Moskal, Janusz,Milart, Piotr

, p. 3201 - 3215 (2007/10/02)

Condensation of various CH-acids of the beta-diketone-type with nitrosobenzene was found to involve a complex sequence of reactions including some reversible processes.The rate-limiting step exhibits second order kinetics and general base catalysis dependence.Structural and solvation effects were considered in terms of the corresponding activation parameters.A detailed mechanism for this condensation is proposed.

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