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137820

Sigma-Aldrich

3-Nitrophthalic acid

99%

Synonym(s):

3-Nitro-1,2-benzenedicarboxylic acid, m-Nitrophthalic acid, o-Nitrophthalic acid

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About This Item

Linear Formula:
O2NC6H3-1,2-(CO2H)2
CAS Number:
Molecular Weight:
211.13
Beilstein/REAXYS Number:
2054269
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

assay

99%

form

powder

mp

210 °C (dec.) (lit.)

solubility

water: soluble 5%, clear to slightly hazy, colorless to faint yellow or tan

SMILES string

OC(=O)c1cccc(c1C(O)=O)[N+]([O-])=O

InChI

1S/C8H5NO6/c10-7(11)4-2-1-3-5(9(14)15)6(4)8(12)13/h1-3H,(H,10,11)(H,12,13)

InChI key

KFIRODWJCYBBHY-UHFFFAOYSA-N

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General description

3-Nitrophthalic acid is a degradation product of isoxaben herbicide. It acts as ligand and forms rare-earth complexes.

Application

3-Nitrophthalic acid was used as starting reagent in the synthesis of modified 2-iodoxybenzoic acid derivatives.

pictograms

CorrosionExclamation mark

signalword

Danger

Hazard Classifications

Eye Dam. 1 - 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


Certificates of Analysis (COA)

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Fan Zhang et al.
Guang pu xue yu guang pu fen xi = Guang pu, 29(10), 2773-2776 (2009-12-30)
A series of rare-earth compound RE2L2 (HL)2 (H2O)6 x 2H2O (RE=La, Nd, Eu, Tb, Er, Y) containing 3-nitrophthalic acid (H2L) ligand were synthesized from ethanol-water solution, and characterized and investigated by the element analysis, infrared and ultraviolet absorption spectra and
Clyatt E Drakeford et al.
Chemosphere, 50(9), 1243-1247 (2003-01-28)
Commercial production of ornamental plants is an important industry in the United States and involves a complex technology that includes the use of herbicides. Isoxaben[N-[3-(1-ethyl-1-methylpropyl)-5-isoxazolyl]-2,6-dimethoxybenzamide] is a pre-emergence herbicide used for controlling weeds in many areas including containerized ornamental plants.
Hypervalent iodine reagents for the oxidation of alcohols and their application to complex molecule synthesis.
Tohma H and Kita Y.
Advanced Synthesis & Catalysis, 346(2-3), 111-124 (2004)
En-Cui Yang et al.
Dalton transactions (Cambridge, England : 2003), 44(7), 3190-3199 (2015-01-13)
Four new 4-amino-1,2,4-triazole (atr)-based coordination polymers, {[Cu2(atr)(H2O)(μ-OH)2(pa)]·H2O}n (), {[Cu3(atr)2(H2O)2(μ-OH)2(npa)2]·2H2O}n (), {[Cu3(atr)5(dca)(μ-OH)(ClO4)2](ClO4)2}n () and {[Cu3(atr)2(H2O)(μ3-OH)(μ-OH)2(spa)]·1.5H2O}n () (pa(2-) = phthalate, npa(2-) = 3-nitrophthalate, dca(-) = dicyanamide and spa(3-) = 4-sulfophthalate), were successfully obtained by varying the carboxylate- and cyanide-modified magnetic bridges. Structural

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