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23985-95-7

Benzo[h]-1,6-naphthyridin-5(6H)-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 23985-95-7 Structure

  • Basic information

    1. Product Name: Benzo[h]-1,6-naphthyridin-5(6H)-one
    2. Synonyms:
    3. CAS NO:23985-95-7
    4. Molecular Formula: C12H8N2O
    5. Molecular Weight: 196.208
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 23985-95-7.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: Benzo[h]-1,6-naphthyridin-5(6H)-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: Benzo[h]-1,6-naphthyridin-5(6H)-one(23985-95-7)
    11. EPA Substance Registry System: Benzo[h]-1,6-naphthyridin-5(6H)-one(23985-95-7)

  • 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: 23985-95-7(Hazardous Substances Data)

23985-95-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 23985-95-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,3,9,8 and 5 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 23985-95:
(7*2)+(6*3)+(5*9)+(4*8)+(3*5)+(2*9)+(1*5)=147
147 % 10 = 7
So 23985-95-7 is a valid CAS Registry Number.

23985-95-7Downstream Products

23985-95-7Relevant articles and documents

Synthesis of new flat polyheterocyclic systems potential DNA intercalating agents diazines part 47

Audoux, Jerome,Achelle, Sylvain,Turck, Alain,Marsais, Francis,Ple, Nelly

, p. 1497 - 1503 (2006)

Using a regioselective metallation in connection with Stille cross-coupling reaction, we report here an original synthetic route to obtain in few steps various flat tetra- or pentaheterocyclic compounds which could be potential intercalating DNA agents.

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