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882529-02-4

2-benzoyl-1-[4-(phenoxathiin-2-yl)phthalazin-1-yl]hydrazine is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 882529-02-4 Structure

  • Basic information

    1. Product Name: 2-benzoyl-1-[4-(phenoxathiin-2-yl)phthalazin-1-yl]hydrazine
    2. Synonyms:
    3. CAS NO:882529-02-4
    4. Molecular Formula:
    5. Molecular Weight: 462.532
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 882529-02-4.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: 2-benzoyl-1-[4-(phenoxathiin-2-yl)phthalazin-1-yl]hydrazine(CAS DataBase Reference)
    10. NIST Chemistry Reference: 2-benzoyl-1-[4-(phenoxathiin-2-yl)phthalazin-1-yl]hydrazine(882529-02-4)
    11. EPA Substance Registry System: 2-benzoyl-1-[4-(phenoxathiin-2-yl)phthalazin-1-yl]hydrazine(882529-02-4)

  • 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: 882529-02-4(Hazardous Substances Data)

882529-02-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 882529-02-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,2,5,2 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 882529-02:
(8*8)+(7*8)+(6*2)+(5*5)+(4*2)+(3*9)+(2*0)+(1*2)=194
194 % 10 = 4
So 882529-02-4 is a valid CAS Registry Number.

882529-02-4Downstream Products

882529-02-4Relevant articles and documents

Synthesis of S-triazolo[3,4-a]phthalazine and related polynuclear heterocyclic systems

Aly,Gad El-Karim

, p. 1997 - 2011 (2005)

The applicability and synthetic potency of the novel reagent 1-hydrazinophthalazine 1 to develop an expeditious convenient synthetic route via the annelation reactions with appropriate reagents for polyfunctionally substituted triazoles, pyrazoles, tetrazoles, and polycyclic condensed systems are reported. Chemical and spectroscopic study for the structures of the newly synthesized compounds are investigated. The prepared compounds were tested in vitro for their antimicrobial activity. Copyright Taylor & Francis Inc.

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