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Home Nitro Compounds 89898-96-4
89898-96-4,MFCD09999191
Catalog No.:AA00IFSU

89898-96-4 | 7-Nitro-2(1h)-quinoxalinone

Pack Size
Purity
Availability
Price(USD)
Quantity
  
100mg
97%
in stock  
$17.00   $12.00
- +
250mg
95%
in stock  
$26.00   $18.00
- +
500mg
95%
in stock  
$45.00   $32.00
- +
1g
95%
in stock  
$76.00   $54.00
- +
2g
95%
in stock  
$150.00   $105.00
- +
5g
95%
in stock  
$334.00   $234.00
- +
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Upstream Synthesis Route
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA00IFSU
Chemical Name:
7-Nitro-2(1h)-quinoxalinone
CAS Number:
89898-96-4
Molecular Formula:
C8H5N3O3
Molecular Weight:
191.1436
MDL Number:
MFCD09999191
SMILES:
[O-][N+](=O)c1ccc2c(c1)[nH]c(=O)cn2
Properties
Properties
 
Form:
Solid  
MP:
275-276°C  
Storage:
Keep in dry area;Room Temperature;  

Computed Properties
 
Complexity:
297  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
14  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
XLogP3:
0.6  

Upstream Synthesis Route

[1]JournaloftheBrazilianChemicalSociety,2017,vol.28,#10,p.1874-1878

[2]TetrahedronLetters,1991,vol.32,#10,p.1311-1314

[3]JournalofMedicinalChemistry,2016,vol.59,#13,p.6169-6186

[4]JournalofMedicinalChemistry,2011,vol.54,#13,p.4508-4522

[1]YakugakuZasshi,1959,vol.79,p.658

[2]Chem.Abstr.,1959,p.21979

[3]JustusLiebigsAnnalenderChemie,1953,vol.579,p.212,220

[4]JournaloftheChemicalSociety,1956,p.26,27

[5]JournaloftheChemicalSociety,1961,p.1246,1250

[1]ChemicalandPharmaceuticalBulletin,2007,vol.55,#2,p.255-267

[2]YakugakuZasshi,1959,vol.79,p.658

[3]Chem.Abstr.,1959,p.21979

[1]JournaloftheAmericanChemicalSociety,1949,vol.71,p.6,7

[1]JournaloftheChemicalSociety,1956,p.26,27

[2]JustusLiebigsAnnalenderChemie,1953,vol.579,p.212,220

[3]YakugakuZasshi,1959,vol.79,p.658

[4]Chem.Abstr.,1959,p.21979

Downstream Synthesis Route

[1]ChemMedChem,2019,vol.14,p.1933-1939

[2]ChemicalandPharmaceuticalBulletin,2007,vol.55,p.255-267

[3]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1959,vol.79,p.658    Chem.Abstr.,1959,p.21979

[1]JournaloftheChemicalSociety,1956,p.26,27

[2]JustusLiebigsAnnalenderChemie,1953,vol.579,p.212,220

[1]ChemMedChem,2019,vol.14,p.1933-1939

[2]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1959,vol.79,p.658    Chem.Abstr.,1959,p.21979

[3]JournaloftheChemicalSociety,1956,p.26,27

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1959,vol.79,p.658    Chem.Abstr.,1959,p.21979

[2]JustusLiebigsAnnalenderChemie,1953,vol.579,p.212,220

[1]JustusLiebigsAnnalenderChemie,1953,vol.579,p.212,220

Literature

Title: Discovery of nitroheterocycles active against African trypanosomes. In vitro screening and preliminary SAR studies.

Journal: Bioorganic & medicinal chemistry letters 20120715

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SDS
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