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1448856-85-6

C22H20F12NP is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1448856-85-6 Structure

  • Basic information

    1. Product Name: C22H20F12NP
    2. Synonyms: C22H20F12NP
    3. CAS NO:1448856-85-6
    4. Molecular Formula:
    5. Molecular Weight: 557.362
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1448856-85-6.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: C22H20F12NP(CAS DataBase Reference)
    10. NIST Chemistry Reference: C22H20F12NP(1448856-85-6)
    11. EPA Substance Registry System: C22H20F12NP(1448856-85-6)

  • 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: 1448856-85-6(Hazardous Substances Data)

1448856-85-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1448856-85-6 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,4,4,8,8,5 and 6 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1448856-85:
(9*1)+(8*4)+(7*4)+(6*8)+(5*8)+(4*5)+(3*6)+(2*8)+(1*5)=216
216 % 10 = 6
So 1448856-85-6 is a valid CAS Registry Number.

1448856-85-6Relevant articles and documents

Effect of multinuclear copper/aluminum complexes in highly asymmetric conjugate addition of trimethylaluminum to acyclic enones

Endo, Kohei,Hamada, Daisuke,Yakeishi, Sayuri,Shibata, Takanori

, p. 606 - 610 (2013)

Al and friends: Asymmetric conjugate addition of Me3Al to β,β-disubstituted α,β-unsaturated ketones in the presence copper and L1 leads to a highly efficient construction of an all-carbon-substituted chiral quaternary center. This result is the first example of an asymmetric conjugate addition of Me3Al to acyclic enones to give a chiral quaternary carbon center with excellent yield and enantioselectivity under mild reaction conditions. Copyright

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