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[2,3-Bipyridine]-4-carbonitrile, 3-fluoro- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 923012-48-0 Structure
  • Basic information

    1. Product Name: [2,3-Bipyridine]-4-carbonitrile, 3-fluoro-
    2. Synonyms: [2,3-Bipyridine]-4-carbonitrile, 3-fluoro-
    3. CAS NO:923012-48-0
    4. Molecular Formula: C11H6FN3
    5. Molecular Weight: 0
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 923012-48-0.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: [2,3-Bipyridine]-4-carbonitrile, 3-fluoro-(CAS DataBase Reference)
    10. NIST Chemistry Reference: [2,3-Bipyridine]-4-carbonitrile, 3-fluoro-(923012-48-0)
    11. EPA Substance Registry System: [2,3-Bipyridine]-4-carbonitrile, 3-fluoro-(923012-48-0)
  • 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: 923012-48-0(Hazardous Substances Data)

923012-48-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 923012-48-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,2,3,0,1 and 2 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 923012-48:
(8*9)+(7*2)+(6*3)+(5*0)+(4*1)+(3*2)+(2*4)+(1*8)=130
130 % 10 = 0
So 923012-48-0 is a valid CAS Registry Number.

923012-48-0Downstream Products

923012-48-0Relevant articles and documents

The synthesis of three new heterocycles: the pyrido[4,3 or 3,4 or 2,3-c]-1,5-naphthyridines

Cailly, Thomas,Fabis, Frédéric,Legay, Rémi,Oulyadi, Hassan,Rault, Sylvain

, p. 71 - 76 (2007/10/03)

Pyrido[4,3 or 3,4 or 2,3-c]-1,5-naphthyridines were obtained with good yields after chlorodehydroxylation and dehalogenation reactions starting from the parent pyridonaphthyridinones. These pyridonaphthyridinones were synthesized in a two-step procedure using a Suzuki cross-coupling reaction between 2-chloro-3-fluoropyridine and orthocyanopyridylboronic esters followed by a KOH-mediated anionic ring closure.

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