72910
4-Nitrobenzoic acid
purum, ≥98.0% (HPLC)
Synonym(s):
p-Nitrobenzoic acid
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50 G
$32.90
250 G
$38.70
1 KG
$58.10
About This Item
Linear Formula:
O2NC6H4CO2H
CAS Number:
Molecular Weight:
167.12
Beilstein/REAXYS Number:
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.[1]
- For the synthesis of mononuclear zinc carboxylate complexes by reacting with zinc sulfate heptahydrate and NaOH.[2]
- As an additive in the room temperature catalytic Wittig reaction.[3]
signalword
Warning
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2 - Eye Irrit. 2 - Muta. 2 - Repr. 2 - Skin Irrit. 2
Storage Class
13 - Non Combustible Solids
wgk_germany
WGK 2
ppe
dust mask type N95 (US), Eyeshields, Gloves
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Enantioselective Organocatalytic ?-Alkylation of Ketones by SN1-Type Reaction of Alcohols.
Trifonidou M and Kokotos CG
European Journal of Organic Chemistry, 2012(8), 1563-1568 (2012)
Synthesis and characterization of zinc benzoate complexes through combined solid and solution phase reactions.
Karmakar A and Baruah JB
Polyhedron, 27(17), 3409-3416 (2008)
Breaking the ring through a room temperature catalytic Wittig reaction.
O'Brien CJ, et al.
Chemistry?A European Journal , 19(19), 5854-5858 (2013)
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
C M Peres et al.
Applied microbiology and biotechnology, 52(3), 440-445 (1999-12-28)
Although isolated on 4-aminobenzoate, Burkholderia cepacia strain PB4 is also able to grow on 4-nitrobenzoate. Degradation of an equimolar mixture of the nitroaromatic compound 4-nitrobenzoate and its corresponding aminoaromatic derivative 4-aminobenzoate by this strain was investigated. Batch experiments showed that
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