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89067-59-4

O-dibenzylhydroxymatairesinol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 89067-59-4 Structure

  • Basic information

    1. Product Name: O-dibenzylhydroxymatairesinol
    2. Synonyms:
    3. CAS NO:89067-59-4
    4. Molecular Formula:
    5. Molecular Weight: 554.64
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 89067-59-4.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: O-dibenzylhydroxymatairesinol(CAS DataBase Reference)
    10. NIST Chemistry Reference: O-dibenzylhydroxymatairesinol(89067-59-4)
    11. EPA Substance Registry System: O-dibenzylhydroxymatairesinol(89067-59-4)

  • 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: 89067-59-4(Hazardous Substances Data)

89067-59-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 89067-59-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,6 and 7 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 89067-59:
(7*8)+(6*9)+(5*0)+(4*6)+(3*7)+(2*5)+(1*9)=174
174 % 10 = 4
So 89067-59-4 is a valid CAS Registry Number.

89067-59-4Relevant articles and documents

ETUDES DE LIGNANES 7 - SYNTHESES TOTALES DES (+-)-α ET -β-CONIDENDRINES ET DES METHYL (+-)-α ET -β-CONIDENDRALS

Dhal, Robert,Nabi, Yahia,Brown, Eric

, p. 2005 - 2016 (2007/10/02)

Michael addition of the carbanion of the dithian 8 on butenolide, followed by alkylation with the benzylic bromide 11 and regeneration of the ketonic carbonyl group, gave the α,β-disubstituted lactone 13.Reduction of the ketonic carbonyl of the latter usi

SYNTHESE TOTALE DE LA (d,l) α-CONIDENDRINE

Nabi, Yahia,Dhal, Robert,Brown, Eric

, p. 1543 - 1546 (2007/10/02)

Michael addition of the carbanion of the dithian 7 (derived from O-benzylvanillin) on butenolide, afforded the saturated lactone 8.Alkylation of the latter with the benzylic bromide 6, followed by regeneration of the carbonyl group gave the α,β-disubstituted lactone 10.Reduction of the ketonic carbonyl group of compound 10 using NaBH4, followed by treatment with CF3CO2H and catalytic hydrogenolysis afforded (d,l)α-conidendrin 1.

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