461091
4-Nitrobenzoic acid
98%
Synonym(s):
p-Nitrobenzoic acid
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About This Item
Linear Formula:
O2NC6H4CO2H
CAS Number:
Molecular Weight:
167.12
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
200-526-2
Beilstein/REAXYS Number:
973593
MDL number:
Assay:
98%
Form:
solid
Product Name
4-Nitrobenzoic acid, 98%
InChI key
OTLNPYWUJOZPPA-UHFFFAOYSA-N
InChI
1S/C7H5NO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4H,(H,9,10)
SMILES string
OC(=O)c1ccc(cc1)[N+]([O-])=O
assay
98%
form
solid
mp
237-240 °C (lit.)
functional group
carboxylic acid
nitro
Quality Level
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Application
4-Nitrobenzoic acid may be used in the preparation of compounds (I and III) trans-M2(T(i)PB)2L2, where T(i)PB = 2,4,6-triisopropylbenzoate:
- compound I (L = 4-nitrobenzoate and M = Mo)
- compound III (L = 4-nitrobenzoate and M2 = MoW)
General description
4-Nitrobenzoic acid (p-nitrobenzoic acid) is a carboxylic acid derivative. It participates in the biosynthesis of the antibiotic aureothin. Infrared Fourier transform spectroscopic studies suggest that the molecules of 4-nitrobenzoic acid gets adsorbed on the surfaces of fine silver powder as carboxylate.
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Repr. 2 - Skin Irrit. 2
Storage Class
11 - Combustible Solids
wgk
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Diffuse reflectance infrared spectra of 4-nitrobenzoic acid and 4-cyanobenzoic acid self-assembled on fine silver particles.
Soo H, et al.
Applied Spectroscopy, 52(8) (1998)
Emmanuel Chanco et al.
Bioorganic & medicinal chemistry, 22(20), 5569-5577 (2014-06-30)
AurF catalyzes the N-oxidation of p-aminobenzoic acid to p-nitrobenzoic acid in the biosynthesis of the antibiotic aureothin. Here we report the characterization of AurF under optimized conditions to explore its potential use in biocatalysis. The pH optimum of the enzyme
Brian G Alberding et al.
Dalton transactions (Cambridge, England : 2003), 43(29), 11397-11403 (2014-06-17)
From the reactions between Mo2(T(i)PB)4, where T(i)PB = 2,4,6-triisopropylbenzoate and two equivalents of the carboxylic acid LH (LH = 4-nitrobenzoic acid and 4'-nitro[1,1'-biphenyl]-4-carboxylic acid) the compounds trans-M2(T(i)PB)2L2 have been prepared: I (L = 4-nitrobenzoate and M = Mo), II (L
Ulrika Forsman et al.
Nature chemical biology, 6(7), 515-517 (2010-06-08)
Coenzyme Q (Q) is an electron transporter in the respiratory chain and a lipid-soluble antioxidant that decreases in humans with age. Here we show that 4-nitrobenzoate inhibited 4-hydroxybenzoate:polyprenyl transferase (Coq2) in a competitive manner and dose-dependently decreased Q in mammalian
Zhifen Lin et al.
Chemical research in toxicology, 16(10), 1365-1371 (2003-10-21)
Quantitative structure-activity relationship (QSAR) approaches are proposed in this study to predict the joint effects of mixture toxicity. The initial investigation studies the joint effects between cyanogenic toxicants and aldehydes to Photobacterium phosphoreum. Joint effects are found to result from
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