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228575

Sigma-Aldrich

4-Hydroxy-3-nitrobenzoic acid

98%

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About This Item

Linear Formula:
HOC6H3(NO2)CO2H
CAS Number:
616-82-0
Molecular Weight:
183.12
Beilstein/REAXYS Number:
2213134
EC Number:
210-494-1
MDL number:
MFCD00007119
UNSPSC Code:
12352100
PubChem Substance ID:
24853695
NACRES:
NA.22

Quality Level

100

assay

98%

form

solid

mp

183-186 °C (lit.)

functional group

carboxylic acid
nitro

SMILES string

OC(=O)c1ccc(O)c(c1)[N+]([O-])=O

InChI

1S/C7H5NO5/c9-6-2-1-4(7(10)11)3-5(6)8(12)13/h1-3,9H,(H,10,11)

InChI key

QRYSWXFQLFLJTC-UHFFFAOYSA-N

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General description

4-Hydroxy-3-nitrobenzoic acid was coupled to ionic liquid-immobilized o-phenylenediamine to form benzimidazole derivatives.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves

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Certificates of Analysis (COA)

Lot/Batch Number
STBJ9864
STBJ9537
STBH7690
STBH7449
STBF9825V

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Kaushik Chanda et al.
ACS combinatorial science, 14(2), 115-123 (2012-01-24)
A novel and efficient diversity-oriented synthetic approach was employed to access the benzo[d]oxazol-5-yl-1H-benzo[d]imidazole on ionic liquid support, which helps to absorb microwave irradiation. In this paper, we successfully coupled 4-hydroxy-3-nitrobenzoic acid onto ionic liquid-immobilized o-phenylenediamine, which subsequently underwent an acid
Yuefei Ji et al.
Water research, 123, 249-257 (2017-07-04)
As promising in-situ chemical oxidation (ISCO) technologies, sulfate radical-based advanced oxidation processes (SR-AOPs) are applied in wastewater treatment and groundwater remediation in recent years. In this contribution, we report for the first time that, thermally activated persulfate oxidation of phenol

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