103608
3-Nitrophenylacetic acid
99%
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About This Item
Linear Formula:
O2NC6H4CH2CO2H
CAS Number:
Molecular Weight:
181.15
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
217-512-7
Beilstein/REAXYS Number:
2050088
MDL number:
Assay:
99%
Form:
solid
Product Name
3-Nitrophenylacetic acid, 99%
InChI key
WUKHOVCMWXMOOA-UHFFFAOYSA-N
InChI
1S/C8H7NO4/c10-8(11)5-6-2-1-3-7(4-6)9(12)13/h1-4H,5H2,(H,10,11)
SMILES string
OC(=O)Cc1cccc(c1)[N+]([O-])=O
assay
99%
form
solid
mp
117-120 °C (lit.)
functional group
carboxylic acid
nitro
Quality Level
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Application
3-Nitrophenylacetic acid was used to study photodecarboxylation of nitrophenylacetate ions in aqueous solution. 3-Nitrophenylacetic acid was used in study to synthesize an azobenzene amino acid, having potent use as photo-inducible conformational switch in polypeptides.
General description
3-Nitrophenylacetic acid is obtained by mild oxidation of 4-amino phenylacetic acid using potassium peroxymonosulfate as oxidizing agent in acetone.
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
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
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Photodecarboxylation of nitrophenylacetate ions.
Margerum JD and Petrusis CT.
Journal of the American Chemical Society, 91(10), 2467-2472 (1969)
A mild oxidation of aromatic amines.
Webb KS and Seneviratne S.
Tetrahedron Letters, 36(14), 2377-2378 (1995)
Andreas Aemissegger et al.
Nature protocols, 2(1), 161-167 (2007-04-03)
The synthesis of an azobenzene amino acid (aa) for use as a photo-inducible conformational switch in polypeptides is described. The compound can be easily incorporated into an aa sequence by solid-phase peptide synthesis using standard 9-fluorenylmethoxycarbonyl methods. A reversible conformational
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