4244-37-5,MFCD13192318
Catalog No.:AA00CH7D

4244-37-5 | 6-Nitroquinoxaline-2-carboxylic acid

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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
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  • Download SDS
Technical Information
Catalog Number:
AA00CH7D
Chemical Name:
6-Nitroquinoxaline-2-carboxylic acid
CAS Number:
4244-37-5
Molecular Formula:
C9H5N3O4
Molecular Weight:
219.1537
MDL Number:
MFCD13192318
SMILES:
[O-][N+](=O)c1ccc2c(c1)ncc(n2)C(=O)O
Properties

Downstream Synthesis Route

[1]CurrentPatentAssignee:NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH;UNIVERSITYOFCLERMONTAUVERGNE-WO2008/12782,2008,A2Locationinpatent:Page/Pagecolumn41-42

[2]Locationinpatent:experimentalpartChezal,Jean-Michel;Papon,Janine;Labarre,Pierre;Lartigue,Claire;Galmier,Marie-Josephe;Decombat,Caroline;Chavignon,Olivier;Maublant,Jean;Teulade,Jean-Claude;Madelmont,Jean-Claude;Moins,Nicole[JournalofMedicinalChemistry,2008,vol.51,#11,p.3133-3144]

[3]CurrentPatentAssignee:LABORATOIRESCYCLOPHARMA;UNIVERSITYOFCLERMONTAUVERGNE;NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH;COMMISSARIATAL'ENERGIEATOMIQUEETAUXENERGIESALTERNATIVES-EP2085390,2009,A1Locationinpatent:Page/Pagecolumn18-19

[4]Desai,SulakshaR.;Desai,VidyaG.;Pissurlenkar,RaghuvirR.[BioorganicChemistry,2022,vol.120]

[5]Desai,SulakshaR.;Desai,VidyaG.;Pissurlenkar,RaghuvirR.[BioorganicChemistry,2022,vol.120]

Literature
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Tags:4244-37-5 Molecular Formula|4244-37-5 MDL|4244-37-5 SMILES|4244-37-5 6-Nitroquinoxaline-2-carboxylic acid
Catalog No.: AA00CH7D
4244-37-5,MFCD13192318
4244-37-5 | 6-Nitroquinoxaline-2-carboxylic acid
This product is typically in stock,please click "Inquire" below or contact us at [email protected]for pricing and availability information.
Inquire
Technical Information
Catalog Number: AA00CH7D
Chemical Name: 6-Nitroquinoxaline-2-carboxylic acid
CAS Number: 4244-37-5
Molecular Formula: C9H5N3O4
Molecular Weight: 219.1537
MDL Number: MFCD13192318
SMILES: [O-][N+](=O)c1ccc2c(c1)ncc(n2)C(=O)O
Properties
Downstream Synthesis Route
64-17-5    4244-37-5    4244-38-6 

[1]CurrentPatentAssignee:NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH;UNIVERSITYOFCLERMONTAUVERGNE-WO2008/12782,2008,A2Locationinpatent:Page/Pagecolumn41-42

[2]Locationinpatent:experimentalpartChezal,Jean-Michel;Papon,Janine;Labarre,Pierre;Lartigue,Claire;Galmier,Marie-Josephe;Decombat,Caroline;Chavignon,Olivier;Maublant,Jean;Teulade,Jean-Claude;Madelmont,Jean-Claude;Moins,Nicole[JournalofMedicinalChemistry,2008,vol.51,#11,p.3133-3144]

[3]CurrentPatentAssignee:LABORATOIRESCYCLOPHARMA;UNIVERSITYOFCLERMONTAUVERGNE;NATIONALINSTITUTEOFHEALTHANDMEDICALRESEARCH;COMMISSARIATAL'ENERGIEATOMIQUEETAUXENERGIESALTERNATIVES-EP2085390,2009,A1Locationinpatent:Page/Pagecolumn18-19

[4]Desai,SulakshaR.;Desai,VidyaG.;Pissurlenkar,RaghuvirR.[BioorganicChemistry,2022,vol.120]

[5]Desai,SulakshaR.;Desai,VidyaG.;Pissurlenkar,RaghuvirR.[BioorganicChemistry,2022,vol.120]

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