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Details

Stereochemistry ACHIRAL
Molecular Formula C8H7NO4
Molecular Weight 181.1455
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of O-NITROPHENYLACETIC ACID

SMILES

OC(=O)CC1=CC=CC=C1[N+]([O-])=O

InChI

InChIKey=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)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Comparative analysis of inhibitory effects of caged ligands for the NMDA receptor.
2005 Mar 15
Mechanisms of cholinesterase inhibition by inorganic mercury.
2007 Apr
Studies of decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl (CNB) caged compounds.
2008 Jan
Leveraging a small-molecule modification to enable the photoactivation of rho GTPases.
2009 Dec 14
Competition between cleavage and decarboxylation in photolysis of alpha-carboxy-2-nitrobenzyl protected cysteine derivatives.
2009 Jun 14
5-(3-Nitro-benz-yl)-1,3,4-thia-diazol-2-amine.
2009 Nov 25
Total synthesis of (+/-)- and (-)-actinophyllic acid.
2010 Apr 7
Delta9-tetrahydrocannabinol is a full agonist at CB1 receptors on GABA neuron axon terminals in the hippocampus.
2010 Jul-Aug
(2-Nitrophenyl)acetyl: a new, selectively removable hydroxyl protecting group.
2010 May 7
The α,5-dicarboxy-2-nitrobenzyl caging group, a tool for biophysical applications with improved hydrophilicity: synthesis, photochemical properties and biological characterization.
2010 Nov-Dec
Inhibition of human carboxylesterases hCE1 and hiCE by cholinesterase inhibitors.
2013 Mar 25
Patents
Name Type Language
O-NITROPHENYLACETIC ACID
Systematic Name English
NITROPHENYLACETIC ACID, O-
Common Name English
(2-NITROPHENYL)ACETIC ACID
Systematic Name English
NSC-16624
Code English
BENZENEACETIC ACID, 2-NITRO-
Systematic Name English
ACETIC ACID, (O-NITROPHENYL)-
Common Name English
2-NITROBENZENEACETIC ACID
Systematic Name English
2-(O-NITROPHENYL)ACETIC ACID
Common Name English
2-(2-NITROPHENYL)ACETIC ACID
Systematic Name English
Code System Code Type Description
CAS
3740-52-1
Created by admin on Fri Dec 15 17:46:55 GMT 2023 , Edited by admin on Fri Dec 15 17:46:55 GMT 2023
PRIMARY
FDA UNII
05TN0SUY38
Created by admin on Fri Dec 15 17:46:55 GMT 2023 , Edited by admin on Fri Dec 15 17:46:55 GMT 2023
PRIMARY
PUBCHEM
77337
Created by admin on Fri Dec 15 17:46:55 GMT 2023 , Edited by admin on Fri Dec 15 17:46:55 GMT 2023
PRIMARY
ECHA (EC/EINECS)
223-128-0
Created by admin on Fri Dec 15 17:46:55 GMT 2023 , Edited by admin on Fri Dec 15 17:46:55 GMT 2023
PRIMARY
EPA CompTox
DTXSID0063157
Created by admin on Fri Dec 15 17:46:55 GMT 2023 , Edited by admin on Fri Dec 15 17:46:55 GMT 2023
PRIMARY
NSC
16624
Created by admin on Fri Dec 15 17:46:55 GMT 2023 , Edited by admin on Fri Dec 15 17:46:55 GMT 2023
PRIMARY