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CAS

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74453-96-6

methyl o--methyl benzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 74453-96-6 Structure

  • Basic information

    1. Product Name: methyl o--methyl benzoate
    2. Synonyms:
    3. CAS NO:74453-96-6
    4. Molecular Formula:
    5. Molecular Weight: 388.51
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 74453-96-6.mol
    9. Article Data: 1

  • 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: methyl o--methyl benzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl o--methyl benzoate(74453-96-6)
    11. EPA Substance Registry System: methyl o--methyl benzoate(74453-96-6)

  • 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: 74453-96-6(Hazardous Substances Data)

74453-96-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 74453-96-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,4,4,5 and 3 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 74453-96:
(7*7)+(6*4)+(5*4)+(4*5)+(3*3)+(2*9)+(1*6)=146
146 % 10 = 6
So 74453-96-6 is a valid CAS Registry Number.

74453-96-6Relevant articles and documents

Antarafacial role of an aromatic nucleus; a novel regiospecific [π4a + π2a] intramolecular cycloaddition of the ene-ketene with an aromatic ring

Kuzuya, Masayuki,Miyake, Fumio,Okuda, Takachiyo

, p. 1043 - 1046 (2007/10/02)

The thermally generated ene-ketene undergoes a facile and regiospecific intramolecular cycloaddition with N,N-dimethylaniline to result in the novel formation of the azulenone derivative via a norcaradiene intermediate.

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