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  • 250328-10-0 Structure
  • Basic information

    1. Product Name: C29H44SO4
    2. Synonyms: C29H44SO4
    3. CAS NO:250328-10-0
    4. Molecular Formula:
    5. Molecular Weight: 488.732
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 250328-10-0.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: C29H44SO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C29H44SO4(250328-10-0)
    11. EPA Substance Registry System: C29H44SO4(250328-10-0)
  • 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: 250328-10-0(Hazardous Substances Data)

250328-10-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 250328-10-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,0,3,2 and 8 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 250328-10:
(8*2)+(7*5)+(6*0)+(5*3)+(4*2)+(3*8)+(2*1)+(1*0)=100
100 % 10 = 0
So 250328-10-0 is a valid CAS Registry Number.

250328-10-0Relevant articles and documents

A convergent and highly efficient synthesis of (E,Z)-2,13-octadecadienyl acetate and (E,Z)-3,13-octadecadienyl acetate, components of the sex pheromone of the Leopard Moth Zeuzera pyrina, through sulfones

Capdevila, Anna,Prasad, Attaluri R.,Quero, Carmen,Petschen, Ine?s,Bosch, Maria P.,Guerrero, Angel

, p. 845 - 848 (2008/02/09)

(equation presented) A new, convergent synthesis of (E,Z)-2,13-octadecadienyl acetate (1) and (E,Z)-3,13-octadecadienyl acetate (2), the two key components of the leopard moth Zeuzera pyrina, from 2-chloromethyltetrahydrofuran in good overall yields and stereomeric purity is reported. The synthesis of both components utilizes the common intermediate sulfone 12 as a convenient building block to be coupled with iodoacetylenic derivatives 9 or 17 in the key step.

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