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CAS

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93716-69-9

2-(4-nitrophenyl)-2,3-dihydro-1,4-phthalazinedione is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 93716-69-9 Structure

  • Basic information

    1. Product Name: 2-(4-nitrophenyl)-2,3-dihydro-1,4-phthalazinedione
    2. Synonyms: 2-(4-nitrophenyl)-2,3-dihydro-1,4-phthalazinedione;4-hydroxy-2-{4-nitrophenyl}-1(2H)-phthalazinone
    3. CAS NO:93716-69-9
    4. Molecular Formula: C14H9N3O4
    5. Molecular Weight: 283.23896
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 93716-69-9.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-(4-nitrophenyl)-2,3-dihydro-1,4-phthalazinedione(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-(4-nitrophenyl)-2,3-dihydro-1,4-phthalazinedione(93716-69-9)
    11. EPA Substance Registry System: 2-(4-nitrophenyl)-2,3-dihydro-1,4-phthalazinedione(93716-69-9)

  • 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: 93716-69-9(Hazardous Substances Data)

93716-69-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 93716-69-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,1 and 6 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93716-69:
(7*9)+(6*3)+(5*7)+(4*1)+(3*6)+(2*6)+(1*9)=159
159 % 10 = 9
So 93716-69-9 is a valid CAS Registry Number.

93716-69-9Relevant articles and documents

Preparation of the N-substituted 1,4-phthalazinedione derivatives

Baloniak,Mroczkiewicz,Katrusiak

, p. 1274 - 1278 (2007/10/03)

Preparation of 1,4-phthalazinedione derivatives from N-aminophthalimide derivatives by condensation of phthalic anhydride with arylhydrazines or isomerization of N-aminophthalimides is described.

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