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About This Item
Linear Formula:
O2NC6H4CH2CO2H
CAS Number:
Molecular Weight:
181.15
Beilstein:
1959243
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
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Quality Level
Assay
98%
form
solid
mp
137-140 °C (lit.)
functional group
carboxylic acid
nitro
SMILES string
OC(=O)Cc1ccccc1[N+]([O-])=O
InChI
1S/C8H7NO4/c10-8(11)5-6-3-1-2-4-7(6)9(12)13/h1-4H,5H2,(H,10,11)
InChI key
WMUZDBZPDLHUMW-UHFFFAOYSA-N
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Related Categories
Application
2-Nitrophenylacetic acid was used as an internal standard in the determination of the theophylline solubilizer salicylamide-O-acetic acid[1].
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
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Leveraging a small-molecule modification to enable the photoactivation of rho GTPases.
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Chembiochem : a European journal of chemical biology, 10(18), 2855-2857 (2009-10-31)
H U Schulz et al.
Journal of pharmaceutical and biomedical analysis, 3(5), 469-475 (1985-01-01)
A high-performance liquid chromatographic method for the determination of the theophylline solubilizer salicylamide-O-acetic acid has been developed in the range 0.5 to 10 microg/ml for human serum and 5 to 400 microg/ml for urine. Reversed-phase ion-pair chromatography was employed with
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Several recent studies have examined the possibility of producing tumor-specific cytotoxicity with various enzyme/ prodrug combinations. The enzymes are targeted to tumor cells either with antibodies (ADEPT, antibody directed enzyme prodrug therapy) or with viruses (VDEPT). The goal of the
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The poorly known mechanism of inhibition of cholinesterases by inorganic mercury (HgCl2) has been studied with a view to using these enzymes as biomarkers or as biological components of biosensors to survey polluted areas. The inhibition of a variety of
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Femtosecond spectroscopy and quantum chemical calculations provide detailed insights into the specificities of the uncaging mechanism of CO2 from ortho-, meta-, and para-nitrophenylacetate. The emerging general principles allow a rational design of improved ortho-nitrophenyl cages for chemical and biological applications.
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