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219631-08-0

6-benzyl pyrazolo<3,4-d>pyridazin-7(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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  • 219631-08-0 Structure

  • Basic information

    1. Product Name: 6-benzyl pyrazolo<3,4-d>pyridazin-7(6H)one
    2. Synonyms:
    3. CAS NO:219631-08-0
    4. Molecular Formula:
    5. Molecular Weight: 226.238
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 219631-08-0.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-benzyl pyrazolo<3,4-d>pyridazin-7(6H)one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-benzyl pyrazolo<3,4-d>pyridazin-7(6H)one(219631-08-0)
    11. EPA Substance Registry System: 6-benzyl pyrazolo<3,4-d>pyridazin-7(6H)one(219631-08-0)

  • 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: 219631-08-0(Hazardous Substances Data)

219631-08-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 219631-08-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,1,9,6,3 and 1 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 219631-08:
(8*2)+(7*1)+(6*9)+(5*6)+(4*3)+(3*1)+(2*0)+(1*8)=130
130 % 10 = 0
So 219631-08-0 is a valid CAS Registry Number.

219631-08-0Downstream Products

219631-08-0Relevant articles and documents

Synthesis and anti-HSV-1 activity of 6 substituted pyrazolo[3,4- d]pyridazin-7-one nucleosides

Baraldi,Manfredini,Romagnoli,Stevanato,Zaid,Manservigi

, p. 2165 - 2173 (1998)

A new series of 6-substituted N1- and N2 -β-D-ribofuranosyl- pyrazolo[3,4-d]pyridazin-7(6H)-one derivatives (8a-g, 9b-d and 9f-g) has been prepared in the aim to explore the structure-activity relationships and improve the antiviral

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