130249
2-Nitrophenylacetic acid
98%
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
O2NC6H4CH2CO2H
CAS Number:
Molecular Weight:
181.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
223-128-0
Beilstein/REAXYS Number:
1959243
MDL number:
Product Name
2-Nitrophenylacetic acid, 98%
InChI key
WMUZDBZPDLHUMW-UHFFFAOYSA-N
InChI
1S/C8H7NO4/c10-8(11)5-6-3-1-2-4-7(6)9(12)13/h1-4H,5H2,(H,10,11)
SMILES string
OC(=O)Cc1ccccc1[N+]([O-])=O
assay
98%
form
solid
mp
137-140 °C (lit.)
functional group
carboxylic acid
nitro
Quality Level
Looking for similar products? Visit Product Comparison Guide
Related Categories
Application
2-Nitrophenylacetic acid was used as an internal standard in the determination of the theophylline solubilizer salicylamide-O-acetic acid.
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
新产品
This item has
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
M K Danks et al.
Clinical cancer research : an official journal of the American Association for Cancer Research, 5(4), 917-924 (1999-04-23)
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
Leveraging a small-molecule modification to enable the photoactivation of rho GTPases.
Katryn R Harwood et al.
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
Manuela F Frasco et al.
The FEBS journal, 274(7), 1849-1861 (2007-03-16)
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
Jan-Michael Mewes et al.
Chemphyschem : a European journal of chemical physics and physical chemistry, 12(11), 2077-2080 (2011-06-10)
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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service