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CAS

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1615240-26-0

ethyl 2-cinnamyl-3-methyl-2H-azirine-2-carboxylate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1615240-26-0 Structure

  • Basic information

    1. Product Name: ethyl 2-cinnamyl-3-methyl-2H-azirine-2-carboxylate
    2. Synonyms: ethyl 2-cinnamyl-3-methyl-2H-azirine-2-carboxylate
    3. CAS NO:1615240-26-0
    4. Molecular Formula:
    5. Molecular Weight: 243.305
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1615240-26-0.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: ethyl 2-cinnamyl-3-methyl-2H-azirine-2-carboxylate(CAS DataBase Reference)
    10. NIST Chemistry Reference: ethyl 2-cinnamyl-3-methyl-2H-azirine-2-carboxylate(1615240-26-0)
    11. EPA Substance Registry System: ethyl 2-cinnamyl-3-methyl-2H-azirine-2-carboxylate(1615240-26-0)

  • 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: 1615240-26-0(Hazardous Substances Data)

1615240-26-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1615240-26-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,6,1,5,2,4 and 0 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1615240-26:
(9*1)+(8*6)+(7*1)+(6*5)+(5*2)+(4*4)+(3*0)+(2*2)+(1*6)=130
130 % 10 = 0
So 1615240-26-0 is a valid CAS Registry Number.

1615240-26-0Downstream Products

1615240-26-0Relevant articles and documents

Transition-metal-free synthesis of substituted pyridines via ring expansion of 2-allyl-2H-azirines

Jiang, Yaojia,Park, Cheol-Min,Loh, Teck-Peng

supporting information, p. 3432 - 3435 (2014/07/21)

A new strategy to open the 2-allyl-2H-azirines by 1,8-diazabicyclo[5.4.0] undec-7-ene (DBU) promotion in metal-free conditions affording 1-azatrienes that in situ electrocyclize to the pyridines in good to excellent yields is reported. The reaction displays a broad substrate scope and good tolerance to a variety of substituents including aryl, alkyl, and heterocyclic groups. In addition, one-pot synthesis of pyridines from oximes via in situ formation of 2H-azirines was achieved.

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