25408
2-Chloro-3-nitrobenzoic acid
purum, ≥98.0% (T)
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About This Item
Linear Formula:
ClC6H3(NO2)CO2H
CAS Number:
Molecular Weight:
201.56
EC Number:
223-590-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
645427
MDL number:
grade
purum
assay
≥98.0% (T)
mp
183-187 °C
SMILES string
OC(=O)c1cccc(c1Cl)[N+]([O-])=O
InChI
1S/C7H4ClNO4/c8-6-4(7(10)11)2-1-3-5(6)9(12)13/h1-3H,(H,10,11)
InChI key
JRQDVRIQJJPHEQ-UHFFFAOYSA-N
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General description
2-Chloro-3-nitrobenzoic acid undergoes condensation with aminoquinolines to yield phenylquinolylamines.
Application
2-Chloro-3-nitrobenzoic acid has been used in the preparation of:
- carboxylic diphenylamines via Ullmann condensation reaction with either 5-amino-7-methoxy-2,2-dimethyl-2H-chromene or 5-amino-2,2-dimethyl-2H-chromene
- new biprivileged molecular scaffolds of tetracyclic indolo-benzodiazepines and indolo-quinoxalines
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A Elomri et al.
Chemical & pharmaceutical bulletin, 47(11), 1604-1606 (1999-12-22)
Condensation of 2-chloro-3-nitrobenzoic acid with either 5-amino-7-methoxy-2,2-dimethyl-2H-chromene or 5-amino-2,2-dimethyl-2H-chromene afforded diphenylamines 14 and 15. Trifluoroacetic anhydride mediated cyclization gave the corresponding acridones 16 and 17, which were subsequently N-methylated and reduced to 11-aminoacronycine and 11-amino-6-demethoxyacronycine. These two amino compounds, which
Indrajeet J Barve et al.
Chemistry, an Asian journal, 7(7), 1684-1690 (2012-04-19)
The present article describes the design and synthesis of new biprivileged molecular scaffolds with diverse structural features. Commercially available, simple heterocyclic building blocks such as 4-fluoro-3-nitrobenzoic acid, 2-chloro-3-nitrobenzoic acid, and indoline were utilized for the synthesis of the novel heterocycles.
J B Bongui et al.
Chemical & pharmaceutical bulletin, 49(9), 1077-1080 (2001-09-18)
Condensation of either 2-bromobenzoic acid (4) or 2-chloro-3-nitrobenzoic acid (5) with suitable aminoquinolines 6-8 afforded phenylquinolylamines 9-13. Acid mediated cyclization gave the corresponding 12H-benzo[b][1,7]phenanthrolin-7-ones 14 and 15, and 12H-benzo[b][1,10]phenanthrolin-7-ones 16-18. Compounds 14, 16, and 17 were subsequently N-methylated to 6-demethoxyacronycine
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