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CAS

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1312719-50-8

6-(4-(phenyl)piperazine-1-yl)-3(2H)-pyridazinone-2-ylacetohydrazide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 1312719-50-8 Structure

  • Basic information

    1. Product Name: 6-(4-(phenyl)piperazine-1-yl)-3(2H)-pyridazinone-2-ylacetohydrazide
    2. Synonyms: 6-(4-(phenyl)piperazine-1-yl)-3(2H)-pyridazinone-2-ylacetohydrazide
    3. CAS NO:1312719-50-8
    4. Molecular Formula:
    5. Molecular Weight: 328.374
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 1312719-50-8.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-(4-(phenyl)piperazine-1-yl)-3(2H)-pyridazinone-2-ylacetohydrazide(CAS DataBase Reference)
    10. NIST Chemistry Reference: 6-(4-(phenyl)piperazine-1-yl)-3(2H)-pyridazinone-2-ylacetohydrazide(1312719-50-8)
    11. EPA Substance Registry System: 6-(4-(phenyl)piperazine-1-yl)-3(2H)-pyridazinone-2-ylacetohydrazide(1312719-50-8)

  • 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: 1312719-50-8(Hazardous Substances Data)

1312719-50-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1312719-50-8 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,2,7,1 and 9 respectively; the second part has 2 digits, 5 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1312719-50:
(9*1)+(8*3)+(7*1)+(6*2)+(5*7)+(4*1)+(3*9)+(2*5)+(1*0)=128
128 % 10 = 8
So 1312719-50-8 is a valid CAS Registry Number.

1312719-50-8Relevant articles and documents

Synthesis, molecular modelling and biological activity of some pyridazinone derivatives as selective human monoamine oxidase-B inhibitors

?zdemir, Zeynep,Alag?z, Mehmet Abdullah,Uslu, Harun,Karakurt, Arzu,Erikci, Acelya,Ucar, Gulberk,Uysal, Mehtap

, p. 692 - 704 (2020/03/11)

Background: Since brain neurotransmitter levels are associated with the pathology of various neurodegenerative diseases like Parkinson and Alzheimer, monoamineoxidase (MAO) plays a critical role in balancing these neurotransmitters in the brain. MAO isofo

The novel synthesized pyridazinone derivates had the antiproliferative and apoptotic effects in SHSY5Y and HEP3B cancer cell line

?iftci, Osman,?zdemir, Zeynep,Acar, Ceren,S?zen, Mert,Ba?ak-Türkmen, Ne?e,Ayhan, ?dris,G?zükara, Harika

, p. 323 - 331 (2018/04/20)

Background: Brain cancer (neuroblastoma) and liver cancer (hepatocellular carcinoma) are common cancer types among others worldwide which do not have a radical treatment and cure. Objective: In the current study, five novel pyridazinone derivates bearing

Synthesis and in vitro antimycobacterial activities of novel 6-substituted-3(2H)-pyridazinone-2-acetyl-2-(substituted/nonsubstituted acetophenone) hydrazone

Utku, Semra,Goekce, Mehtap,Aslan, Goenuel,Bayram, Guel,Uelger, Mahmut,Emekdas, Guerol,Sahin, M. Fethi

scheme or table, p. 331 - 339 (2011/12/16)

The difficulty in managing tuberculosis includes the prolonged duration of the treatment, the emergence of drug resistance, and coinfection with HIV/AIDS. Tuberculosis control requires new drugs that act on novel drug targets to help in combating resistan

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