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1364265-60-0

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

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  • 1364265-60-0 Structure

  • Basic information

    1. Product Name: 1-benzoyl-5-methyl-1H-indol-3-yl acetate
    2. Synonyms:
    3. CAS NO:1364265-60-0
    4. Molecular Formula:
    5. Molecular Weight: 293.322
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1364265-60-0.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: 1-benzoyl-5-methyl-1H-indol-3-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzoyl-5-methyl-1H-indol-3-yl acetate(1364265-60-0)
    11. EPA Substance Registry System: 1-benzoyl-5-methyl-1H-indol-3-yl acetate(1364265-60-0)

  • 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: 1364265-60-0(Hazardous Substances Data)

1364265-60-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1364265-60-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,6,4,2,6 and 5 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1364265-60:
(9*1)+(8*3)+(7*6)+(6*4)+(5*2)+(4*6)+(3*5)+(2*6)+(1*0)=160
160 % 10 = 0
So 1364265-60-0 is a valid CAS Registry Number.

1364265-60-0Downstream Products

1364265-60-0Relevant articles and documents

A trans diacyloxylation of indoles

Liu, Qiang,Zhao, Qing Yong,Liu, Jie,Wu, Pan,Yi, Hong,Lei, Aiwen

, p. 3239 - 3241 (2012)

A trans diacyloxylation of indoles is accomplished by employing PhI(OAc)2 as the oxidant. A broad range of functional groups are well tolerated. Both the electronic properties of the N-protecting groups of indoles and the acidity of the reaction media play important roles in the selectivity of indole acyloxylation reactions. The Royal Society of Chemistry 2012.

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