72915
Sodium 3-nitrobenzoate
≥95.0% (HPLC)
Sinônimo(s):
3-Nitrobenzoic acid sodium salt
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About This Item
Fórmula linear:
3-O2NC6H4CO2Na
Número CAS:
Peso molecular:
189.10
Beilstein:
4166479
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22
Produtos recomendados
Ensaio
≥95.0% (HPLC)
forma
solid
cadeia de caracteres SMILES
[Na+].[O-]C(=O)c1cccc(c1)[N+]([O-])=O
InChI
1S/C7H5NO4.Na/c9-7(10)5-2-1-3-6(4-5)8(11)12;/h1-4H,(H,9,10);/q;+1/p-1
chave InChI
MUADFEZFSKAZLT-UHFFFAOYSA-M
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Aplicação
Sodium 3-nitrobenzoate may be used in the synthesis of [Ni(cyclam)(3-nitrobenzoate)2] complex. [Cyclam = 1,4,8,11-tetraazacyclotetradecane]
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Novel nickel cyclam complexes with potent antimicrobial and cytotoxic properties.
Al-Bari MAA
Journal of Applied Sciences Research, 3(11), 1251-1261 (2007)
Miguel A Providenti et al.
Applied and environmental microbiology, 72(4), 2651-2660 (2006-04-07)
In Comamonas sp. strain JS46, 3-nitrobenzoate (3Nba) is initially oxidized at the 3,4 position by a dioxygenase, which results in release of nitrite and production of protocatechuate. The locus coding for the 3Nba dioxygenase (designated mnb, for m-nitrobenzoate) was mobilized
M Samsonowicz et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 82(1), 235-246 (2011-08-25)
The influence of beryllium, magnesium, calcium, strontium and barium cations on the electronic system of 3-nitrobenzoic acid was studied in comparison with studied earlier alkali metal ions. The vibrational FT-IR (in KBr and ATR techniques) and (1)H and (13)C NMR
Zhiqiang Hu et al.
Water research, 39(4), 710-720 (2005-02-15)
The physical and biochemical characteristics of the biomass in three lab-scale sequencing batch reactors (SBR) treating a synthetic wastewater at a 20-day target solids retention time (SRT) were investigated. The synthetic wastewater feed contained biogenic compounds and 22 organic priming
C R Bloom et al.
Biochemistry, 37(31), 10937-10944 (1998-08-07)
The positive and negative cooperativity and apparent half-site reactivity of the Co(II)-substituted insulin hexamer are well-described by a three-state allosteric model involving ligand-mediated interconversions between the three states: T3T3' right harpoon over left harpoon T3o R3o right harpoon over left
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