Home Bromides 116529-61-4
116529-61-4,MFCD10700064
Catalog No.:AA000CMR

116529-61-4 | 3-Bromo-2-nitrobenzoic acid

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1g
95%
in stock  
$62.00   $44.00
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10g
98%
in stock  
$610.00   $427.00
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25g
98%
in stock  
$1,208.00   $846.00
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  • 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:
AA000CMR
Chemical Name:
3-Bromo-2-nitrobenzoic acid
CAS Number:
116529-61-4
Molecular Formula:
C7H4BrNO4
Molecular Weight:
246.0150
MDL Number:
MFCD10700064
SMILES:
[O-][N+](=O)c1c(Br)cccc1C(=O)O
NSC Number:
108607
Properties
Computed Properties
 
Complexity:
227  
Covalently-Bonded Unit Count:
1  
Heavy Atom Count:
13  
Hydrogen Bond Acceptor Count:
4  
Hydrogen Bond Donor Count:
1  
Rotatable Bond Count:
1  
XLogP3:
2  

Upstream Synthesis Route

[1]JournaloftheChineseChemicalSociety,2014,vol.61,#12,p.1307-1312

[2]JustusLiebigsAnnalenderChemie,1869,vol.149,p.142

[3]RecueildesTravauxChimiquesdesPays-Bas,1901,vol.20,p.215,225

[4]JustusLiebigsAnnalenderChemie,1884,vol.222,p.115

[5]JustusLiebigsAnnalenderChemie,1867,vol.143,p.241

[6]RecueildesTravauxChimiquesdesPays-Bas,1901,vol.20,p.215,225

[7]JustusLiebigsAnnalenderChemie,1912,vol.388,p.34

[8]JustusLiebigsAnnalenderChemie,1912,vol.388,p.34

[9]RecueildesTravauxChimiquesdesPays-Bas,1901,vol.20,p.215,225

[10]JustusLiebigsAnnalenderChemie,1867,vol.143,p.241

[11]ChemicalCommunications,2010,vol.46,#24,p.4360-4362

[12]AngewandteChemie-InternationalEdition,2018,vol.57,#42,p.13805-13809

[13]Angew.Chem.,2018,vol.130,#42,p.14001-14005,5

[1]RecueildesTravauxChimiquesdesPays-Bas,1926,vol.45,p.531

[2]JournaloftheChemicalSociety,1928,p.451

[1]JustusLiebigsAnnalenderChemie,1867,vol.143,p.241

[2]JustusLiebigsAnnalenderChemie,1869,vol.149,p.142

[3]JustusLiebigsAnnalenderChemie,1884,vol.222,p.104

[1]Patent:CN103880683,2018,B,.Locationinpatent:Paragraph0014;0024;0029-0030;0041;0052

[1]AdvancedSynthesisandCatalysis,2015,vol.357,#14-15,p.3303-3308

[2]JournalofOrganicChemistry,1940,vol.5,p.606,608

[3]JournaloftheChemicalSociety,1929,p.2742

[4]JournaloftheChemicalSociety,1926,p.1803

[5]JournalofOrganicChemistry,2010,vol.75,#23,p.8224-8233

Downstream Synthesis Route

[1]JustusLiebigsAnnalenderChemie,1867,vol.143,p.241

[1]JournaloftheChineseChemicalSociety,2014,vol.61,p.1307-1312

[2]JustusLiebigsAnnalenderChemie,1869,vol.149,p.142

[3]RecueildesTravauxChimiquesdesPays-Bas,1901,vol.20,p.215,225

[4]JustusLiebigsAnnalenderChemie,1912,vol.388,p.34

[5]JustusLiebigsAnnalenderChemie,1912,vol.388,p.34

[6]RecueildesTravauxChimiquesdesPays-Bas,1901,vol.20,p.215,225

[7]ChemicalCommunications,2010,vol.46,p.4360-4362

[8]AngewandteChemie-InternationalEdition,2018,vol.57,p.13805-13809    Angew.Chem.,2018,vol.130,p.14001-14005,5

[1]AdvancedSynthesisandCatalysis,2015,vol.357,p.3303-3308

[2]JournalofOrganicChemistry,1940,vol.5,p.606,608

[3]JournaloftheChemicalSociety,1929,p.2742

[4]JournalofOrganicChemistry,2010,vol.75,p.8224-8233

[1]JournalofOrganicChemistry,1940,vol.5,p.606,608

[1]JustusLiebigsAnnalenderChemie,1867,vol.143,p.241

[2]JustusLiebigsAnnalenderChemie,1869,vol.149,p.142

Literature
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SDS
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