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146512-56-3

2-[1-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 2-[1-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile

    Cas No: 146512-56-3

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  • 146512-56-3 Structure

  • Basic information

    1. Product Name: 2-[1-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile
    2. Synonyms: 2-[1-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile
    3. CAS NO:146512-56-3
    4. Molecular Formula:
    5. Molecular Weight: 227.266
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 146512-56-3.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-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[1-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile(146512-56-3)
    11. EPA Substance Registry System: 2-[1-Methyl-imidazolidin-(2E)-ylidene]-3-oxo-3-phenyl-propionitrile(146512-56-3)

  • 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: 146512-56-3(Hazardous Substances Data)

146512-56-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 146512-56-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,6,5,1 and 2 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 146512-56:
(8*1)+(7*4)+(6*6)+(5*5)+(4*1)+(3*2)+(2*5)+(1*6)=123
123 % 10 = 3
So 146512-56-3 is a valid CAS Registry Number.

146512-56-3Downstream Products

146512-56-3Relevant articles and documents

A new route to 3H-1,5-benzodiazepines and heterocyclic ketene animals from benzoyl substituted ketene dithioacetals and diamines

Huang,Wang

, p. 1273 - 1276 (2007/10/02)

Heterocyclic ketene aminals 5 or 3H-1,5-benzodiazepines 4 were obtained from the reaction of benzoyl substituted ketene dithioacetals 1 with various diamines 2. The mechanism of formation of these two different products are discussed.

SYNTHESE UND REAKTIONEN NEUARTIGER N-VINYLAZIRIDINE

Rudorf, W.-D.

, p. 1791 - 1799 (2007/10/02)

The ketene S,S-acetals 1 readily react with aziridine to give the corresponding 3-(1-aziridinyl)-3-methylthio-acrylnitriles 2 and 3,3-bis-(1-aziridinyl)-acrylnitriles 3.Ketene S,N-acetals 4 yield 3-anilino-3-(1-aziridinyl)-acrylnitriles 5.Reaction of 5 with potassium iodide in acetone at room temperature leads to imidazolidines 8.The isomerisation is explained in terms of a two-step mechanism.The iodide ion-catalysed rearrangement was not successful when applied to 2a.Cyclisation of 5b in the presence of sodium hydride and following hydrolysis form the tautomeric quinolone 10.On contrary to 1 and 4 mercapto ethylenes 11 and 13 with aziridine give the thiazolidine 15.

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