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438536-22-2

nootkatone-11,12-epoxide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 438536-22-2 Structure

  • Basic information

    1. Product Name: nootkatone-11,12-epoxide
    2. Synonyms:
    3. CAS NO:438536-22-2
    4. Molecular Formula:
    5. Molecular Weight: 234.338
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 438536-22-2.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: nootkatone-11,12-epoxide(CAS DataBase Reference)
    10. NIST Chemistry Reference: nootkatone-11,12-epoxide(438536-22-2)
    11. EPA Substance Registry System: nootkatone-11,12-epoxide(438536-22-2)

  • 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: 438536-22-2(Hazardous Substances Data)

438536-22-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 438536-22-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,3,8,5,3 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 438536-22:
(8*4)+(7*3)+(6*8)+(5*5)+(4*3)+(3*6)+(2*2)+(1*2)=162
162 % 10 = 2
So 438536-22-2 is a valid CAS Registry Number.

438536-22-2Upstream product

438536-22-2Downstream Products

438536-22-2Relevant articles and documents

Microbial transformation of (+)-nootkatone and the antiproliferative activity of its metabolites

Gliszczyńska, Anna,?ysek, Agnieszka,Janeczko, Tomasz,?witalska, Marta,Wietrzyk, Joanna,Wawrzeńczyk, Czes?aw

experimental part, p. 2464 - 2469 (2011/05/12)

Six metabolites were obtained as a result of microbial transformation of (+)-nootkatone (1) by the fungal strains: Botrytis, Didymosphaeria, Aspergillus, Chaetomium and Fusarium. Their structure were established as (+)-(4R,5S,7R,9R)-9α-hydroxynootkatone (2), (+)-(4R,5S,7R)-13- hydroxynootkatone (3) and (+)-(4R,5S,7R,9R,11S)-11,12-epoxy-9α- hydroxynootkatone (4), (+)-(4R,5S,7R,11S)-11,12-epoksynootkatone (5), (+)-(4R,5S,7R)-11,12-dihydroxynootkatone (6) and (+)-(4R,5S,7R)-7,11,12- trihydroxynootkatone (7) on the basis of their spectral data. Two products: (4) and (7) were not previously reported in the literature. The antiproliferative activity of (+)-nootkatone (1) and isolated metabolites (2-7) of its biotransformation has been evaluated.

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