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92218-81-0

1R,4S,5R,9S-4,5-dihydrocaryophyllen-5-ol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 92218-81-0 Structure

  • Basic information

    1. Product Name: 1R,4S,5R,9S-4,5-dihydrocaryophyllen-5-ol
    2. Synonyms: 1R,4S,5R,9S-4,5-dihydrocaryophyllen-5-ol
    3. CAS NO:92218-81-0
    4. Molecular Formula:
    5. Molecular Weight: 222.371
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 92218-81-0.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: 1R,4S,5R,9S-4,5-dihydrocaryophyllen-5-ol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 1R,4S,5R,9S-4,5-dihydrocaryophyllen-5-ol(92218-81-0)
    11. EPA Substance Registry System: 1R,4S,5R,9S-4,5-dihydrocaryophyllen-5-ol(92218-81-0)

  • 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: 92218-81-0(Hazardous Substances Data)

92218-81-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 92218-81-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,2,2,1 and 8 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 92218-81:
(7*9)+(6*2)+(5*2)+(4*1)+(3*8)+(2*8)+(1*1)=130
130 % 10 = 0
So 92218-81-0 is a valid CAS Registry Number.

92218-81-0Upstream product

92218-81-0Relevant articles and documents

REDUCTION OF CARYOPHYLLENE AND ISOCARYOPHYLLENE 4,5-EPOXIDES WITH LITHIUM IN LIQUID AMMONIA

Tkachev, A. V.

, p. 109 - 118 (2007/10/02)

The reduction of the stereoisomeric 4,5-epoxy derivatives of the caryophyllene series with lithium in liquid ammonia gives the products from C-C cyclization with participation of the 8,13-double bond in addition to the "normal" reduction products, i.e., the 4-hydroxy- and 5-hydroxycaryophyllene compounds.The chemical structure and configuration of both the "normal" reduction products and the cyclocaryophyllane compounds containing the tricyclo2,5>undecane skeleton were established by analysis of the 1H and 13C NMR spectra and the optical rotatory dispersion curves.

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