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1577067-67-4

ethyl 2-((phenylamino)(phenyl)methyl)-3-oxohexanoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1577067-67-4 Structure

  • Basic information

    1. Product Name: ethyl 2-((phenylamino)(phenyl)methyl)-3-oxohexanoate
    2. Synonyms:
    3. CAS NO:1577067-67-4
    4. Molecular Formula:
    5. Molecular Weight: 339.434
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1577067-67-4.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: ethyl 2-((phenylamino)(phenyl)methyl)-3-oxohexanoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-((phenylamino)(phenyl)methyl)-3-oxohexanoate(1577067-67-4)
    11. EPA Substance Registry System: ethyl 2-((phenylamino)(phenyl)methyl)-3-oxohexanoate(1577067-67-4)

  • 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: 1577067-67-4(Hazardous Substances Data)

1577067-67-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1577067-67-4 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,5,7,7,0,6 and 7 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1577067-67:
(9*1)+(8*5)+(7*7)+(6*7)+(5*0)+(4*6)+(3*7)+(2*6)+(1*7)=204
204 % 10 = 4
So 1577067-67-4 is a valid CAS Registry Number.

1577067-67-4Downstream Products

1577067-67-4Relevant articles and documents

Metal-free, one-pot, rapid synthesis of tetrahydropyridines using acetic acid as solvent and catalyst at room temperature

Balijapalli, Umamahesh,Munusamy, Sathishkumar,Sundaramoorthy, Karthikeyan Natesan,Iyer, Sathiyanarayanan Kulathu

, p. 943 - 953 (2014)

Acetic acid-promoted, one-pot synthesis of tetrahydropyridines has been developed under metal-catalyst-free conditions via a tandem reaction. High atom economy, good yield, simple procedure, no expensive column chromatography, shorter reaction time, and metal-free and mild reaction conditions are some of the important features of this protocol. The current methodology provides an alternative approach for not only highly substituted tetrahydropyridines (THPs) but also fully substituted tetrahydropyridines (FTHPs) in moderate to good yields. The plausible mechanism for the formation of THPs was greatly promoted by the H+ ion coming from acetic acid. [Supplementary materials are available for this article. Go to the publisher's online edition of Synthetic Communications for the following free supplemental resource(s): Full experimental and spectral details.]

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