72910
4-Nitrobenzoic acid
purum, ≥98.0% (HPLC)
Synonym(s):
p-Nitrobenzoic acid
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About This Item
Linear Formula:
O2NC6H4CO2H
CAS Number:
Molecular Weight:
167.12
Beilstein:
973593
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
grade
purum
Quality Level
Assay
≥98.0% (HPLC)
form
crystals
mp
237-240 °C (lit.)
239-242 °C
functional group
carboxylic acid
nitro
SMILES string
OC(=O)c1ccc(cc1)[N+]([O-])=O
InChI
1S/C7H5NO4/c9-7(10)5-1-3-6(4-2-5)8(11)12/h1-4H,(H,9,10)
InChI key
OTLNPYWUJOZPPA-UHFFFAOYSA-N
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Application
4-Nitrobenzoic acid can be used:
- As a co-catalyst with thioxotetrahydropyrimidinone for the α-alkylation of ketones.
- For the synthesis of mononuclear zinc carboxylate complexes by reacting with zinc sulfate heptahydrate and NaOH.
- As an additive in the room temperature catalytic Wittig reaction.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Repr. 2 - Skin Irrit. 2
Storage Class Code
13 - Non Combustible Solids
WGK
WGK 2
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Breaking the ring through a room temperature catalytic Wittig reaction.
O'Brien CJ, et al.
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Synthesis and characterization of zinc benzoate complexes through combined solid and solution phase reactions.
Karmakar A and Baruah JB
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Jing He et al.
Journal of the American Chemical Society, 126(12), 3694-3695 (2004-03-25)
The antibiotic aureothin is a rare natural nitroaromatic compound produced by Streptomyces thioluteus. By labeling experiments, we demonstrate for the first time that p-nitrobenzoate (PNBA) serves as a polyketide synthase starter unit. Cloning, heterologous expression, and inactivation experiments reveal that
J A Gómez-Vidal et al.
Organic letters, 3(16), 2477-2479 (2001-08-03)
[reaction: see text] A mild and selective cleavage of p-nitrobenzoic esters by sodium azide in methanol is reported. This new methodology is mild enough for use with acid- or base-sensitive compounds. No elimination byproducts are formed. Fmoc- and trifluoroacetyl-amino protecting
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