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1044518-06-0

CF3O3S(1-)*C56H42Cl2NO2(1+) is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1044518-06-0 Structure

  • Basic information

    1. Product Name: CF3O3S(1-)*C56H42Cl2NO2(1+)
    2. Synonyms:
    3. CAS NO:1044518-06-0
    4. Molecular Formula:
    5. Molecular Weight: 980.931
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1044518-06-0.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: CF3O3S(1-)*C56H42Cl2NO2(1+)(CAS DataBase Reference)
    10. NIST Chemistry Reference: CF3O3S(1-)*C56H42Cl2NO2(1+)(1044518-06-0)
    11. EPA Substance Registry System: CF3O3S(1-)*C56H42Cl2NO2(1+)(1044518-06-0)

  • 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: 1044518-06-0(Hazardous Substances Data)

1044518-06-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1044518-06-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,4,4,5,1 and 8 respectively; the second part has 2 digits, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1044518-06:
(9*1)+(8*0)+(7*4)+(6*4)+(5*5)+(4*1)+(3*8)+(2*0)+(1*6)=120
120 % 10 = 0
So 1044518-06-0 is a valid CAS Registry Number.

1044518-06-0Downstream Products

1044518-06-0Relevant articles and documents

Chiral ammonium betaines: A bifunctional organic base catalyst for asymmetric mannich-type reaction of α-nitrocarboxylates

Uraguchi, Daisuke,Koshimoto, Kyohei,Ooi, Takashi

, p. 10878 - 10879 (2008)

A chiral ammonium betaine, an intramolecular ion-pairing quaternary ammonium aryloxide 3, has been designed and its vast potential as an enantioselective organic base catalyst has been successfully demonstrated in the highly enantioselective direct Mannich-type reaction of α-substituted α-nitrocarboxylates 2 with various N-Boc imines 1. The present study provides a conceptually new approach toward the design of bifunctional, chiral quaternary ammonium salts and their utilizations as a homogeneous organic molecular catalyst. Copyright

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