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1206901-03-2

C17H14F3NO4 is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1206901-03-2 Structure

  • Basic information

    1. Product Name: C17H14F3NO4
    2. Synonyms:
    3. CAS NO:1206901-03-2
    4. Molecular Formula:
    5. Molecular Weight: 353.298
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1206901-03-2.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: C17H14F3NO4(CAS DataBase Reference)
    10. NIST Chemistry Reference: C17H14F3NO4(1206901-03-2)
    11. EPA Substance Registry System: C17H14F3NO4(1206901-03-2)

  • 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: 1206901-03-2(Hazardous Substances Data)

1206901-03-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1206901-03-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,0,6,9,0 and 1 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1206901-03:
(9*1)+(8*2)+(7*0)+(6*6)+(5*9)+(4*0)+(3*1)+(2*0)+(1*3)=112
112 % 10 = 2
So 1206901-03-2 is a valid CAS Registry Number.

1206901-03-2Downstream Products

1206901-03-2Relevant articles and documents

Dual heterogeneous catalysis for a regioselective three-component synthesis of Bi-and Tri(hetero)arylpyridines

Allais, Christophe,Lieby-Muller, Frederic,Constantieux, Thierry,Rodriguez, Jean

, p. 2537 - 2544 (2012/10/30)

We have designed a new, user-friendly oxidative dual heterogeneous catalytic system capable of promoting polysubstituted pyridines as unique products from simple activated Michael acceptors, 1,3-dicarbonyls and ammonium acetate. This metal-free environmentally-respectful and totally regioselective domino reaction proved to be a great strategy to access bi- and triaryl-type pyridines as well as challenging bi- and triheteroaryl-type pyridines in a single operation. Copyright

Use of β,γ-unsaturated α-ketocarbonyls for a totally regioselective oxidative multicomponent synthesis of polyfunctionalized pyridines

Allais, Christophe,Constantieux, Thierry,Rodriguez, Jean

supporting information; experimental part, p. 12945 - 12948 (2010/05/19)

Versatile partners: α-Ketocarbonyls have been shown for the first time to be versatile partners in a Michael addition promoted oxidative domino threecomponent reaction under heterogeneous conditions. This multicomponent reaction sequence led to the development of a general synthesis of highly functionalized pyridines (see scheme), allowing selective and simultaneous incorporation of a substituent at the 4-position and a synthetically useful functionality at the strategic 2-position.

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