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CAS

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1146543-40-9

6-(phenyl)pyrrolo[1,2-a][1,6]naphthyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1146543-40-9 Structure

  • Basic information

    1. Product Name: 6-(phenyl)pyrrolo[1,2-a][1,6]naphthyridine
    2. Synonyms: 6-(phenyl)pyrrolo[1,2-a][1,6]naphthyridine
    3. CAS NO:1146543-40-9
    4. Molecular Formula:
    5. Molecular Weight: 244.296
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1146543-40-9.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: 6-(phenyl)pyrrolo[1,2-a][1,6]naphthyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(phenyl)pyrrolo[1,2-a][1,6]naphthyridine(1146543-40-9)
    11. EPA Substance Registry System: 6-(phenyl)pyrrolo[1,2-a][1,6]naphthyridine(1146543-40-9)

  • 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: 1146543-40-9(Hazardous Substances Data)

1146543-40-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1146543-40-9 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,1,4,6,5,4 and 3 respectively; the second part has 2 digits, 4 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1146543-40:
(9*1)+(8*1)+(7*4)+(6*6)+(5*5)+(4*4)+(3*3)+(2*4)+(1*0)=139
139 % 10 = 9
So 1146543-40-9 is a valid CAS Registry Number.

1146543-40-9Downstream Products

1146543-40-9Relevant articles and documents

Synthesis of pyrrolo[1,2-a]naphthyridines by Lewis acid mediated cycloisomerization

Flader, Anika,Parpart, Silvio,Ehlers, Peter,Langer, Peter

, p. 3216 - 3231 (2017)

Pyrrolo[1,2-a]naphthyridines were synthesized from 3-alkynyl-2-([1H]-pyrrol-1-yl)pyridines and 3-alkynyl-4-([1H]-pyrrol-1-yl)pyridines by cycloisomerization. The reactions are performed by application of the Lewis acids PtCl2 or Bi(OTf)3 without the need of further additives. With the described methods a number of derivatives containing a variety of functional groups have been synthesized in up to 78% yield.

Tandem Pd-catalyzed double C-C bond formation: Effect of water

Chai, David I.,Lautens, Mark

supporting information; experimental part, p. 3054 - 3061 (2009/08/07)

A highly efficient water-accelerated palladium-catalyzed reaction of gem-dibromoolefins with a boronic acid via a tandem Suzuki-Miyaura coupling and direct arylation is reported. A wide range of aryl, alkenyl, and alkyl boronic acids, as well as a variety

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