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204512-13-0

3-[(4-Methoxy-phenyl)-hydrazono]-3,4-dihydro-1H-quinoxalin-2-one is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

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  • 204512-13-0 Structure

  • Basic information

    1. Product Name: 3-[(4-Methoxy-phenyl)-hydrazono]-3,4-dihydro-1H-quinoxalin-2-one
    2. Synonyms: 3-[(4-Methoxy-phenyl)-hydrazono]-3,4-dihydro-1H-quinoxalin-2-one
    3. CAS NO:204512-13-0
    4. Molecular Formula:
    5. Molecular Weight: 282.302
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 204512-13-0.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: 3-[(4-Methoxy-phenyl)-hydrazono]-3,4-dihydro-1H-quinoxalin-2-one(CAS DataBase Reference)
    10. NIST Chemistry Reference: 3-[(4-Methoxy-phenyl)-hydrazono]-3,4-dihydro-1H-quinoxalin-2-one(204512-13-0)
    11. EPA Substance Registry System: 3-[(4-Methoxy-phenyl)-hydrazono]-3,4-dihydro-1H-quinoxalin-2-one(204512-13-0)

  • 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: 204512-13-0(Hazardous Substances Data)

204512-13-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 204512-13-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,4,5,1 and 2 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 204512-13:
(8*2)+(7*0)+(6*4)+(5*5)+(4*1)+(3*2)+(2*1)+(1*3)=80
80 % 10 = 0
So 204512-13-0 is a valid CAS Registry Number.

204512-13-0Relevant articles and documents

1,2,4-Triazolo[4,3-a]quinoxalin-1-one moiety as an attractive scaffold to develop new potent and selective human A3 adenosine receptor antagonists: Synthesis, pharmacological, and ligand-receptor modeling studies

Colotta, Vittoria,Catarzi, Daniela,Varano, Flavia,Calabri, Francesca Romana,Lenzi, Ombretta,Filacchioni, Guido,Martini, Claudia,Trincavelli, Letizia,Deflorian, Francesca,Moro, Stefano

, p. 3580 - 3590 (2004)

In the past few years much effort in our laboratory has been directed toward the study of adenosine receptor antagonists, and recently we focused our attention on 2-aryl-1,2,4-triazolo[4,3-a]quinoxaline-1,4-diones and 2- aryl-1,2,4-triazolo[4,3-a]quinoxal

Tricyclic heteroaromatic systems. 1,2,4-Triazolo[4,3-a]quinoxalines and 1,2,4-triazino[4,3-a]quinoxalines: Synthesis and central benzodiazepine receptor activity

Colotta, Vittoria,Catarzi, Daniela,Varano, Flavia,Cecchi, Lucia,Filacchioni, Guido,Galli, Alessandro,Costagli, Chiara

, p. 387 - 391 (2007/10/03)

Some 1,2,4-triazolo[4,3-a]quinoxalines 1-10, and 1,2,4-triazino[4,3-a]quinoxalines 11-12 were prepared and biologically evaluated for their binding at the benzodiazepine receptor (BZR) in rat cortical membranes. The BZR affinity of 1-10 demonstrates that

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