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142088-65-1

5α-(benzyloxymethyl)-1-ethenyl-5β,8aβ-dimethyl-trans-3,4,4a,5,6,7,8,8a-octahydronaphtalene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 142088-65-1 Structure

  • Basic information

    1. Product Name: 5α-(benzyloxymethyl)-1-ethenyl-5β,8aβ-dimethyl-trans-3,4,4a,5,6,7,8,8a-octahydronaphtalene
    2. Synonyms:
    3. CAS NO:142088-65-1
    4. Molecular Formula:
    5. Molecular Weight: 310.48
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 142088-65-1.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: 5α-(benzyloxymethyl)-1-ethenyl-5β,8aβ-dimethyl-trans-3,4,4a,5,6,7,8,8a-octahydronaphtalene(CAS DataBase Reference)
    10. NIST Chemistry Reference: 5α-(benzyloxymethyl)-1-ethenyl-5β,8aβ-dimethyl-trans-3,4,4a,5,6,7,8,8a-octahydronaphtalene(142088-65-1)
    11. EPA Substance Registry System: 5α-(benzyloxymethyl)-1-ethenyl-5β,8aβ-dimethyl-trans-3,4,4a,5,6,7,8,8a-octahydronaphtalene(142088-65-1)

  • 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: 142088-65-1(Hazardous Substances Data)

142088-65-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 142088-65-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,0,8 and 8 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 142088-65:
(8*1)+(7*4)+(6*2)+(5*0)+(4*8)+(3*8)+(2*6)+(1*5)=121
121 % 10 = 1
So 142088-65-1 is a valid CAS Registry Number.

142088-65-1Relevant articles and documents

STUDIES FOR A DIASTEREOSELECTIVE SYNTHESIS OF THE TETRACYCLIC DITERPENIC DIOL STEMARIN. AN IMPROVED PROCEDURE FOR THE SYNTHESIS OF 8(9)-PODOCARPEN-14-ONES: THE TOTAL SYNTHESIS OF 18-BENZYLOXY-8(9)-PODOCARPEN-14-ONE AND RELATED STUDIES

Antonaroli, Simonetta,Berettoni, Marco,Cifarelli, Guido,Lupi, Alessandro,Bettolo, Rinaldo Marini,Romeo, Sergio

, p. 55 - 59 (2007/10/02)

An efficient preparation of 18-benzyloxy-8(9)-podocarpen-14-one, 3a, a key intermediate for a diastereoselective synthesis of the bicyclooctan-2-ol, 1, precursor of the tetracyclic diol stemarin, 2, is described.The approach outlined can be, in principle, applied to the preparation of related compounds.

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