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14400-33-0

3-(4-methoxy-phenyl)-1-methyl-imidazolidin-4-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 14400-33-0 Structure

  • Basic information

    1. Product Name: 3-(4-methoxy-phenyl)-1-methyl-imidazolidin-4-one
    2. Synonyms: 3-(4-methoxy-phenyl)-1-methyl-imidazolidin-4-one
    3. CAS NO:14400-33-0
    4. Molecular Formula:
    5. Molecular Weight: 206.244
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 14400-33-0.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: 3-(4-methoxy-phenyl)-1-methyl-imidazolidin-4-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-(4-methoxy-phenyl)-1-methyl-imidazolidin-4-one(14400-33-0)
    11. EPA Substance Registry System: 3-(4-methoxy-phenyl)-1-methyl-imidazolidin-4-one(14400-33-0)

  • 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: 14400-33-0(Hazardous Substances Data)

14400-33-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14400-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,4,0 and 0 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 14400-33:
(7*1)+(6*4)+(5*4)+(4*0)+(3*0)+(2*3)+(1*3)=60
60 % 10 = 0
So 14400-33-0 is a valid CAS Registry Number.

14400-33-0Upstream product

14400-33-0Downstream Products

14400-33-0Relevant articles and documents

Reaction of N-methylazomethine ylide with aroyl azides: Synthesis of imidazolidin-4-ones

Buev, Evgeny M.,Moshkin, Vladimir S.,Sosnovskikh, Vyacheslav Y.

, p. 773 - 776 (2019)

Aryl isocyanates generated in situ from aroyl azides react with N-methylazomethine ylide generated in situ from N-methylspiroanthraceneoxazolidine at 210 °C in a microwave reactor to form 3-arylimidazolidin-4-ones in 30–81% yield.

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