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245040-42-0

2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 245040-42-0 Structure

  • Basic information

    1. Product Name: 2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one
    2. Synonyms: 2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one
    3. CAS NO:245040-42-0
    4. Molecular Formula:
    5. Molecular Weight: 332.44
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 245040-42-0.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: 2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one(245040-42-0)
    11. EPA Substance Registry System: 2-[(4S,5R)-5-Allyl-2-(4-methoxy-phenyl)-[1,3]dioxan-4-yl]-2-methyl-pentan-3-one(245040-42-0)

  • 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: 245040-42-0(Hazardous Substances Data)

245040-42-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 245040-42-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,5,0,4 and 0 respectively; the second part has 2 digits, 4 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 245040-42:
(8*2)+(7*4)+(6*5)+(5*0)+(4*4)+(3*0)+(2*4)+(1*2)=100
100 % 10 = 0
So 245040-42-0 is a valid CAS Registry Number.

245040-42-0Relevant articles and documents

Design and synthesis of constrained epothilone analogs: The efficient synthesis of eleven-membered rings by olefin metathesis

Winkler, Jeffrey D.,Holland, Joanne M.,Kasparec, Jiri,Axelsen, Paul H.

, p. 8199 - 8214 (2007/10/03)

The efficient synthesis of both left- and right-hand halves of a constrained analog of the anticancer natural product epothilone is described. The eleven-membered rings common to both compounds are prepared by olefin metathesis.

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