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  • 31469-30-4 Structure
  • Basic information

    1. Product Name: tetracosan-2-one
    2. Synonyms: 2-tetracosanone
    3. CAS NO:31469-30-4
    4. Molecular Formula: C24H48O
    5. Molecular Weight: 352.64
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 31469-30-4.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 394.6°C at 760 mmHg
    3. Flash Point: 45.3°C
    4. Appearance: N/A
    5. Density: 0.836g/cm3
    6. Vapor Pressure: 4.44E-06mmHg at 25°C
    7. Refractive Index: 1.449
    8. Storage Temp.: N/A
    9. Solubility: N/A
    10. CAS DataBase Reference: tetracosan-2-one(CAS DataBase Reference)
    11. NIST Chemistry Reference: tetracosan-2-one(31469-30-4)
    12. EPA Substance Registry System: tetracosan-2-one(31469-30-4)
  • 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: 31469-30-4(Hazardous Substances Data)

31469-30-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 31469-30-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,1,4,6 and 9 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 31469-30:
(7*3)+(6*1)+(5*4)+(4*6)+(3*9)+(2*3)+(1*0)=104
104 % 10 = 4
So 31469-30-4 is a valid CAS Registry Number.

31469-30-4Upstream product

31469-30-4Downstream Products

31469-30-4Relevant articles and documents

Extensive isomerization of alkenes using a bifunctional catalyst: An alkene zipper

Grotjahn, Douglas B.,Larsen, Casey R.,Gustafson, Jeffery L.,Nair, Reji,Sharma, Abhinandini

, p. 9592 - 9593 (2008/03/11)

Catalyzed movement of alkene double bonds up to 30 positions has been accomplished using a catalyst featuring a cationic CpRu fragment and bifunctional imidazolylphosphine. The basic nitrogen of the latter is thought to deprotonate coordinated alkene intermediates reversibly, facilitating isomerization between terminal and (E)-alkenes and accelerating conversions by factors of up to 1 × 104. Copyright

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