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(+/-)-Klaineanone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 83914-24-3 Structure
  • Basic information

    1. Product Name: (+/-)-Klaineanone
    2. Synonyms:
    3. CAS NO:83914-24-3
    4. Molecular Formula:
    5. Molecular Weight: 364.439
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 83914-24-3.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: (+/-)-Klaineanone(CAS DataBase Reference)
    10. NIST Chemistry Reference: (+/-)-Klaineanone(83914-24-3)
    11. EPA Substance Registry System: (+/-)-Klaineanone(83914-24-3)
  • 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: 83914-24-3(Hazardous Substances Data)

83914-24-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 83914-24-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,9,1 and 4 respectively; the second part has 2 digits, 2 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 83914-24:
(7*8)+(6*3)+(5*9)+(4*1)+(3*4)+(2*2)+(1*4)=143
143 % 10 = 3
So 83914-24-3 is a valid CAS Registry Number.

83914-24-3Downstream Products

83914-24-3Relevant articles and documents

Total Synthesis of the Highly Oxygenated Quassinoid (+/-)-Klaineanone

Grieco, Paul A.,Nargund, Ravi P.,Parker, David T.

, p. 6287 - 6294 (1989)

The total synthesis of klaineanone (1), isolated from the seeds of Hannoa klaineana, is described in racemic form.The synthesis commences with the tetracyclic ketone 6, which is transformed into tetracyclic olefinic lactone 23, which possesses the correct configuration at C(9).Incorporation of the ring A 1β-hydroxy-2-oxo-Δ3,4 olefin unit into tetracyclic olefinic lactone 23, which features a Rubottom epoxidation of silyloxy diene 35 followed by a base-catalyzed tautomerism of the resultant hydroxy ketone 36, provides tetracyclic olefin 37, Epoxidation of the C(11), C(12) olefin in teracyclic compound 37 and subsequent acid-catalyzed ring opening affords dl-klaineanone.

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