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CAS

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1019996-01-0

3-allyl-1-(4-methoxybenzyl)-2-oxo-2,3-dihydroindol-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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  • 1019996-01-0 Structure

  • Basic information

    1. Product Name: 3-allyl-1-(4-methoxybenzyl)-2-oxo-2,3-dihydroindol-3-yl acetate
    2. Synonyms: 3-allyl-1-(4-methoxybenzyl)-2-oxo-2,3-dihydroindol-3-yl acetate
    3. CAS NO:1019996-01-0
    4. Molecular Formula:
    5. Molecular Weight: 351.402
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1019996-01-0.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: 3-allyl-1-(4-methoxybenzyl)-2-oxo-2,3-dihydroindol-3-yl acetate(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-allyl-1-(4-methoxybenzyl)-2-oxo-2,3-dihydroindol-3-yl acetate(1019996-01-0)
    11. EPA Substance Registry System: 3-allyl-1-(4-methoxybenzyl)-2-oxo-2,3-dihydroindol-3-yl acetate(1019996-01-0)

  • 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: 1019996-01-0(Hazardous Substances Data)

1019996-01-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1019996-01-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,9,9,9 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 1019996-01:
(9*1)+(8*0)+(7*1)+(6*9)+(5*9)+(4*9)+(3*6)+(2*0)+(1*1)=170
170 % 10 = 0
So 1019996-01-0 is a valid CAS Registry Number.

1019996-01-0Downstream Products

1019996-01-0Relevant articles and documents

Catalytic asymmetric hydroxylation of oxindoles by molecular oxygen using a phase-transfer catalyst

Sano, Daisuke,Nagata, Kazuhiro,Itoh, Takashi

, p. 1593 - 1595 (2008)

The highly enantioselective catalytic hydroxylation of 3-substituted oxindoles was achieved by using a phase-transfer catalyst with molecular oxygen as an oxidant. The product then was converted to an optically active compound 8, which was a synthetic precursor of alkaloid CPC-1.

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