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1407804-60-7

methyl 3-acetyl-2-hydroxy-4-methoxy-6-methylbenzoate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1407804-60-7 Structure

  • Basic information

    1. Product Name: methyl 3-acetyl-2-hydroxy-4-methoxy-6-methylbenzoate
    2. Synonyms: methyl 3-acetyl-2-hydroxy-4-methoxy-6-methylbenzoate
    3. CAS NO:1407804-60-7
    4. Molecular Formula:
    5. Molecular Weight: 238.24
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1407804-60-7.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: methyl 3-acetyl-2-hydroxy-4-methoxy-6-methylbenzoate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 3-acetyl-2-hydroxy-4-methoxy-6-methylbenzoate(1407804-60-7)
    11. EPA Substance Registry System: methyl 3-acetyl-2-hydroxy-4-methoxy-6-methylbenzoate(1407804-60-7)

  • 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: 1407804-60-7(Hazardous Substances Data)

1407804-60-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1407804-60-7 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,0,7,8,0 and 4 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1407804-60:
(9*1)+(8*4)+(7*0)+(6*7)+(5*8)+(4*0)+(3*4)+(2*6)+(1*0)=147
147 % 10 = 7
So 1407804-60-7 is a valid CAS Registry Number.

1407804-60-7Relevant articles and documents

Total synthesis of chlorocyclinone A, a PPAR-γ antagonist

Karmakar, Raju,Mal, Dipakranjan

, p. 10235 - 10248 (2012)

The first total synthesis of chlorocyclinone A (1) is regioselectively completed in 28 steps. The key steps are Pd-catalyzed methoxycarbonylation, unprecedented Hauser annulation, Krohn photo-oxidation, and regioselective gem-dichlorination.

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