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419569-93-0

methyl 1-benzyl-5-methoxy-1H-indole-3-acetate is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 419569-93-0 Structure

  • Basic information

    1. Product Name: methyl 1-benzyl-5-methoxy-1H-indole-3-acetate
    2. Synonyms: methyl 1-benzyl-5-methoxy-1H-indole-3-acetate
    3. CAS NO:419569-93-0
    4. Molecular Formula:
    5. Molecular Weight: 309.365
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 419569-93-0.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: methyl 1-benzyl-5-methoxy-1H-indole-3-acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: methyl 1-benzyl-5-methoxy-1H-indole-3-acetate(419569-93-0)
    11. EPA Substance Registry System: methyl 1-benzyl-5-methoxy-1H-indole-3-acetate(419569-93-0)

  • 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: 419569-93-0(Hazardous Substances Data)

419569-93-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 419569-93-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,1,9,5,6 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 419569-93:
(8*4)+(7*1)+(6*9)+(5*5)+(4*6)+(3*9)+(2*9)+(1*3)=190
190 % 10 = 0
So 419569-93-0 is a valid CAS Registry Number.

419569-93-0Relevant articles and documents

Aromatization of 1,6,7,7a-tetrahydro-2H-indol-2-ones by a novel process. Preparation of key-intermediate methyl 1-benzyl-5-methoxy-1H-indole-3-acetate and the syntheses of serotonin, melatonin, and bufotenin

Revial, Gilbert,Jabin, Ivan,Lim, Sethy,Pfau, Michel

, p. 2252 - 2256 (2002)

Imine 7 of 1,4-cyclohexanedione mono-ethylene ketal 6 was reacted with maleic anhydride, affording the cyclized adduct 8. Methyl esterification of 8, accompanied by transacetalization, led to the dihydrooxindole derivative 10. Aromatization of 10 was then accomplished with POCl3, leading directly to the key-intermediate title compound 11 in 74% yield from ketone 6. Serotonin, melatonin, and bufotenin were then obtained by standard reactions.

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