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CAS

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64373-81-5

8α-hydroxyelemol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 64373-81-5 Structure

  • Basic information

    1. Product Name: 8α-hydroxyelemol
    2. Synonyms: 8α-hydroxyelemol
    3. CAS NO:64373-81-5
    4. Molecular Formula:
    5. Molecular Weight: 238.37
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 64373-81-5.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: 8α-hydroxyelemol(CAS DataBase Reference)
    10. NIST Chemistry Reference: 8α-hydroxyelemol(64373-81-5)
    11. EPA Substance Registry System: 8α-hydroxyelemol(64373-81-5)

  • 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: 64373-81-5(Hazardous Substances Data)

64373-81-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 64373-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,4,3,7 and 3 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 64373-81:
(7*6)+(6*4)+(5*3)+(4*7)+(3*3)+(2*8)+(1*1)=135
135 % 10 = 5
So 64373-81-5 is a valid CAS Registry Number.

64373-81-5Downstream Products

64373-81-5Relevant articles and documents

Efficient synthesis of the anticancer β-elemene and other bioactive elemanes from sustainable germacrone

Barrero, Alejandro F.,Herrador, M. Mar,Quilez Del Moral, Jose F.,Arteaga, Pilar,Meine, Niklas,Perez-Morales, M. Carmen,Catalan, Julieta V.

, p. 1118 - 1125 (2011)

Highly efficient preparations of anticancer β-elemene and other bioactive elemanes were carried out using the natural product germacrone as a renewable starting material. The syntheses were achieved in only 3-5 steps with excellent overall yields (43-54%). An enantioselective approach to these molecules is also described

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