Status : experimental

Chemical Classification

This compound belongs to the class of organic compounds known as phenylacetic acid derivatives. These are compounds containing a phenylacetic acid moiety, which consists of a phenyl group substituted at the second position by an acetic acid.

Phenylacetic acid derivatives

Organic compounds


Benzene and substituted derivatives

Phenylacetic acid derivatives

Calculated Property

kind Value Source
logP 1.72 ALOGPS
logS -2.4 ALOGPS
Water Solubility 7.91e-01 g/l ALOGPS
logP 1.55 ChemAxon
IUPAC Name 2-(4-nitrophenyl)acetic acid ChemAxon
Traditional IUPAC Name 2-(4-nitrophenyl)acetic acid ChemAxon
Molecular Weight 181.1455 ChemAxon
Monoisotopic Weight 181.037507717 ChemAxon
SMILES OC(=O)CC1=CC=C(C=C1)[N+]([O-])=O ChemAxon
Molecular Formula C8H7NO4 ChemAxon
InChI InChI=1S/C8H7NO4/c10-8(11)5-6-1-3-7(4-2-6)9(12)13/h1-4H,5H2,(H,10,11) ChemAxon
Polar Surface Area (PSA) 83.12 ChemAxon
Refractivity 44.69 ChemAxon
Polarizability 16.27 ChemAxon
Rotatable Bond Count 3 ChemAxon
H Bond Acceptor Count 4 ChemAxon
H Bond Donor Count 1 ChemAxon
pKa (strongest acidic) 3.07 ChemAxon
pKa (strongest basic) -9.7 ChemAxon
Physiological Charge -1 ChemAxon
Number of Rings 1 ChemAxon
Bioavailability 1 ChemAxon
Rule of Five 1 ChemAxon
Ghose Filter 1 ChemAxon
MDDR-Like Rule 0 ChemAxon

Target within organism

  • Penicillin G acylase : in Escherichia coli