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81278-14-0

N-methyl-N-(o-allylbenzoyl)-2-phenylglycine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 81278-14-0 Structure

  • Basic information

    1. Product Name: N-methyl-N-(o-allylbenzoyl)-2-phenylglycine
    2. Synonyms: N-methyl-N-(o-allylbenzoyl)-2-phenylglycine
    3. CAS NO:81278-14-0
    4. Molecular Formula:
    5. Molecular Weight: 309.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 81278-14-0.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: N-methyl-N-(o-allylbenzoyl)-2-phenylglycine(CAS DataBase Reference)
    10. NIST Chemistry Reference: N-methyl-N-(o-allylbenzoyl)-2-phenylglycine(81278-14-0)
    11. EPA Substance Registry System: N-methyl-N-(o-allylbenzoyl)-2-phenylglycine(81278-14-0)

  • 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: 81278-14-0(Hazardous Substances Data)

81278-14-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81278-14-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,7 and 8 respectively; the second part has 2 digits, 1 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81278-14:
(7*8)+(6*1)+(5*2)+(4*7)+(3*8)+(2*1)+(1*4)=130
130 % 10 = 0
So 81278-14-0 is a valid CAS Registry Number.

81278-14-0Downstream Products

81278-14-0Relevant articles and documents

Regiochemistry of Intramolecular Munchnone Cycloadditions: Preparative and Mechanistic Implications

Padwa, Albert,Gingrich, Henry L.,Lim, Richard

, p. 2447 - 2456 (2007/10/02)

A series of munchnone derivatives containing an internal ? bond were generated in situ by treating several N-(o-allylphenyl)alanines with acetic anhydride.The major product obtained corresponded to intramolecular 1,3-dipolar cycloaddition of the mesoionic

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