125113
2-Chloro-5-nitrobenzoic acid
97%
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About This Item
Linear Formula:
ClC6H3(NO2)CO2H
CAS Number:
Molecular Weight:
201.56
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
219-739-7
Beilstein/REAXYS Number:
1877474
MDL number:
Product Name
2-Chloro-5-nitrobenzoic acid, 97%
InChI key
QUEKGYQTRJVEQC-UHFFFAOYSA-N
InChI
1S/C7H4ClNO4/c8-6-2-1-4(9(12)13)3-5(6)7(10)11/h1-3H,(H,10,11)
SMILES string
OC(=O)c1cc(ccc1Cl)[N+]([O-])=O
assay
97%
form
powder
mp
165-168 °C (lit.)
functional group
carboxylic acid
chloro
nitro
Quality Level
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General description
2-Chloro-5-nitrobenzoic acid undergoes microwave-assisted, regioselective amination reaction with aliphatic and aromatic amines to yield N-substituted 5-nitroanthranilic acid derivatives. It acts as ligand and forms a red luminescent one dimensional coordination polymer with Eu(III).
wgk
WGK 1
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Sens. 1
Storage Class
11 - Combustible Solids
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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2-Chloro-5-nitrobenzoato complexes of Eu (III) and Tb (III)-A 1D coordination polymer and enhanced solution luminescence.
Viswanathan S and Bettencourt-Dias A.
Inorganic Chemistry Communications, 9(5), 444-448 (2006)
Younis Baqi et al.
The Journal of organic chemistry, 72(15), 5908-5911 (2007-06-26)
The synthesis of N-substituted 5-nitroanthranilic acid derivatives 3a-w was achieved by a new, mild, microwave-assisted, regioselective amination reaction of 5-nitro-2-chlorobenzoic acid (1a) with a diverse range of aliphatic and aromatic amines 2a-w without added solvent or catalyst. Up to >99%
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