Home Nitro Compounds 25084-14-4
25084-14-4,MFCD00039564
Catalog No.:AA002QDA

25084-14-4 | 2-Furancarbonyl chloride, 5-nitro-

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1g
95%
in stock  
$124.00   $87.00
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5g
95%
in stock  
$307.00   $215.00
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25g
95%
in stock  
$1,129.00   $790.00
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  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
  • Request for Quotation
  • Download SDS
  • Technical Information
  • Properties
  • Downstream Synthesis Route
  • Literature
Technical Information
Catalog Number:
AA002QDA
Chemical Name:
2-Furancarbonyl chloride, 5-nitro-
CAS Number:
25084-14-4
Molecular Formula:
C5H2ClNO4
Molecular Weight:
175.5267
MDL Number:
MFCD00039564
SMILES:
ClC(=O)c1ccc(o1)[N+](=O)[O-]
NSC Number:
74620
Properties
Properties
 
Form:
Solid  
MP:
34-41℃  

Computed Properties
 
Complexity:
189  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
11  
Hydrogen Bond Acceptor Count:
4  
Rotatable Bond Count:
1  
XLogP3:
2  

Downstream Synthesis Route
25084-14-4    144-80-9   
5-nitro-furan-2-carboxylicacid-(4-acetylsulfamoyl-anilide) 

[1]YakugakuZasshi/JournalofthePharmaceuticalSocietyofJapan,1949,vol.69,p.289    Chem.Abstr.,1950,p.5373

[1]Patent:WO2017/17631,2017,A2.Locationinpatent:Paragraph00312;00314

[2]Patent:US2011/86817,2011,A1.Locationinpatent:Page/Pagecolumn5

[3]CollectionofCzechoslovakChemicalCommunications,1994,vol.59,p.1400-1407

[4]IndianJournalofChemistry-SectionBOrganicandMedicinalChemistry,1987,vol.26,p.856-860

[5]JournalofMedicinalChemistry,2004,vol.47,p.5276-5283

[6]JournaloftheChemicalSociety.PerkinTransactions2(2001),2001,p.2211-2218

[7]BioorganicandMedicinalChemistryLetters,2007,vol.17,p.6714-6719

[8]JournalofMedicinalChemistry,2008,vol.51,p.3094-3103

[9]Patent:WO2005/7625,2005,A2.Locationinpatent:Page47-48

[10]Patent:WO2005/7625,2005,A2.Locationinpatent:Page68

[11]BioorganicandMedicinalChemistry,2011,vol.19,p.816-825

[12]Molecules,2011,vol.16,p.2023-2031

[13]JournalofMedicinalChemistry,2012,vol.55,p.697-708

[14]ChemicalandPharmaceuticalBulletin,2012,vol.60,p.764-771

[15]JournalofMedicinalChemistry,2013,vol.56,p.796-806

[16]BioorganicandMedicinalChemistry,2014,vol.22,p.1938-1947

[17]JournaloftheAmericanChemicalSociety,2015,vol.137,p.1448-1451

[18]EuropeanJournalofMedicinalChemistry,2017,vol.125,p.1088-1097

[19]ScientiaPharmaceutica,2018,vol.86

[20]ChemMedChem,2019,vol.14,p.1227-1231

25084-14-4    6973-09-7   
5-Nitro-furan-2-carboxylicacid(4-methyl-3-sulfamoyl-phenyl)-amide 

[1]OrganicPreparationsandProceduresInternational,1997,vol.29,p.671-677

696-45-7    25084-14-4   
5-nitro-furan-2-carboxylicacid(6-methoxy-pyrimidin-4-yl)-amide 

[1]JournalofMedicinalChemistry,2004,vol.47,p.5276-5283

[2]Patent:WO2005/7625,2005,A2.Locationinpatent:Page49

25084-14-4    5464-79-9   
5-nitro-furan-2-carboxylicacid(4-methoxy-benzothiazol-2-yl)-amide 

[1]JournalofMedicinalChemistry,2004,vol.47,p.5276-5283

[2]Patent:WO2005/7625,2005,A2.Locationinpatent:Page49

[3]Patent:US2005/222408,2005,A1

Literature

Title: Drug resistance modulation in Staphylococcus aureus, a new biological activity for mesoionic hydrochloride compounds.

Journal: Molecules (Basel, Switzerland) 20110227

Title: Quantitative structure-activity relationship and complex network approach to monoamine oxidase A and B inhibitors.

Journal: Journal of medicinal chemistry 20081113

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