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1-benzyl-11bβ-methyl-2aβ,3,5aβ,8,9,10,11,11aα,11b,11cβ-decahydro-2H-isoxazolo <5,4,3-k,l> benzo quinolizin-6-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

81454-39-9

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  • 81454-39-9 Structure

  • Basic information

    1. Product Name: 1-benzyl-11bβ-methyl-2aβ,3,5aβ,8,9,10,11,11aα,11b,11cβ-decahydro-2H-isoxazolo <5,4,3-k,l> benzo quinolizin-6-one
    2. Synonyms:
    3. CAS NO:81454-39-9
    4. Molecular Formula:
    5. Molecular Weight: 338.45
    6. EINECS: N/A
    7. Product Categories: N/A

  • 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-benzyl-11bβ-methyl-2aβ,3,5aβ,8,9,10,11,11aα,11b,11cβ-decahydro-2H-isoxazolo <5,4,3-k,l> benzo quinolizin-6-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1-benzyl-11bβ-methyl-2aβ,3,5aβ,8,9,10,11,11aα,11b,11cβ-decahydro-2H-isoxazolo <5,4,3-k,l> benzo quinolizin-6-one(81454-39-9)
    11. EPA Substance Registry System: 1-benzyl-11bβ-methyl-2aβ,3,5aβ,8,9,10,11,11aα,11b,11cβ-decahydro-2H-isoxazolo <5,4,3-k,l> benzo quinolizin-6-one(81454-39-9)

  • 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: 81454-39-9(Hazardous Substances Data)

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81454-39-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 81454-39-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,4,5 and 4 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 81454-39:
(7*8)+(6*1)+(5*4)+(4*5)+(3*4)+(2*3)+(1*9)=129
129 % 10 = 9
So 81454-39-9 is a valid CAS Registry Number.

81454-39-9Downstream Products

81454-39-9Relevant academic research and scientific papers

INTRAMOLECULAR CYCLOADDITIONS OF NITRONES JOINED BY AMIDES TO OLEFINS

Brambilla, R.,Friary, R.,Ganguly, A.,Puar, M. S.,Sunday, B. R.,et al.

, p. 3615 - 3625 (2007/10/02)

Six nitrones joined by amides to olefins were prepared in situ from related ketones 1-3 with N-methyl- and benzylhydroxylamines.The nitrones added intramolecularly to the olefins, and the cycloadditions gave the 6-lactams 4-9 stereoselectively and regiosp

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