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10-phenyl-benzo-1,5-naphthyridine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21820-08-6

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  • 21820-08-6 Structure
  • Basic information

    1. Product Name: 10-phenyl-benzo-1,5-naphthyridine
    2. Synonyms: 10-phenyl-benzo-1,5-naphthyridine
    3. CAS NO:21820-08-6
    4. Molecular Formula:
    5. Molecular Weight: 286.376
    6. EINECS: N/A
    7. Product Categories: N/A
  • 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: 10-phenyl-benzo-1,5-naphthyridine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 10-phenyl-benzo-1,5-naphthyridine(21820-08-6)
    11. EPA Substance Registry System: 10-phenyl-benzo-1,5-naphthyridine(21820-08-6)
  • 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: 21820-08-6(Hazardous Substances Data)

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21820-08-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 21820-08-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,8,2 and 0 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 21820-08:
(7*2)+(6*1)+(5*8)+(4*2)+(3*0)+(2*0)+(1*8)=76
76 % 10 = 6
So 21820-08-6 is a valid CAS Registry Number.

21820-08-6Downstream Products

21820-08-6Relevant academic research and scientific papers

Synthesis of a benzo[b]-1,5-naphthyridine derivative as a potential constrained NK1 receptor antagonist

Viti, Giovanni,Giannotti, Danilo,Nannicini, Rossano,Balacco, Giuseppe,Pestellini, Vittorio

, p. 5939 - 5942 (1994)

A short synthesis of a cyclic constrained analogue 1 of the potent Substance P antagonist (±) CP-96345 is described. The key feature is the formation of the benzo[b]-1,5-naphthyridine system at the very last step of the synthesis through an intramolecular arylation of an amine promoted by a strong base. If the tricyclic system was synthesized first, 2-methoxy benzylation of both the nitrogen atoms occurred.

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