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Details

Stereochemistry ACHIRAL
Molecular Formula C7H7NO3
Molecular Weight 153.1354
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of P-NITROANISOLE

SMILES

COC1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=BNUHAJGCKIQFGE-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5H,1H3

HIDE SMILES / InChI

Molecular Formula C7H7NO3
Molecular Weight 153.1354
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Formation of epoxide-amine oligo-adducts as OH-functionalized initiators for the ring-opening polymerization of ε-caprolactone.
2010-10-01
Structure and vibrational frequencies of 6,7-dimethoxy-1,4-dihydro-1,3-quinoxalinedione based on density functional theory calculations: The role of pi-electron conjugation and back-donation.
2010-09-15
Mechanisms underlying the inhibition of the cytochrome P450 system by copper ions.
2009-11
Alteration in metabolism and toxicity of acetaminophen upon repeated administration in rats.
2009-10
Simulation of IR and Raman spectra of p-hydroxyanisole and p-nitroanisole based on scaled DFT force fields and their vibrational assignments.
2009-09-15
Differentiating solvation mechanisms at polar solid/liquid interfaces.
2009-05-06
RNA interference-mediated knockdown of a cytochrome P450, CYP6BG1, from the diamondback moth, Plutella xylostella, reduces larval resistance to permethrin.
2009-01
The element effect and nucleophilicity in nucleophilic aromatic photosubstitution (SN2Ar*). Local atom effects as mechanistic probes of very fast reactions.
2008-03-07
Enhanced aqueous photochemical reaction rates after freezing.
2007-11-01
Induction of hepatic CYP2E1 by a subtoxic dose of acetaminophen in rats: increase in dichloromethane metabolism and carboxyhemoglobin elevation.
2007-10
The element effect in nucleophilic aromatic photosubstitution (SN2Ar*).
2007-07-19
Effects of dimethylsulfoxide on metabolism and toxicity of acetaminophen in mice.
2006-08
Determination of Kamlet-Taft solvent parameters pi* of high pressure and supercritical water by the UV-Vis absorption spectral shift of 4-nitroanisole.
2006-05-21
New nitronate sigma complexes and the mechanism of nucleophilic aromatic photosubstitution para to a nitro group.
2006-03-30
Absence of beta-catenin alteration in hepatic tumors induced by p-nitroanisole in Crj:BDF1 mice.
2006
Determination of molar absorption coefficients of organic compounds adsorbed in porous media.
2005-12
Photodegradation of organic compounds adsorbed in porous mineral layers: determination of quantum yields.
2005-09-01
Correlation between fenvalerate resistance and cytochrome P450-mediated O-demethylation activity in Helicoverpa armigera (Lepidoptera: Noctuidae).
2005-06
Essential role of singlet oxygen species in cytochrome P450-dependent substrate oxygenation by rat liver microsomes.
2005-02
Degradation of 4-nitrophenol by the lignin-degrading basidiomycete Phanerochaete chrysosporium.
2004-12
The involvement of microsomal oxidases in pyrethroid resistance in Helicoverpa armigera from Asia.
2004-08
Application of vicarious nucleophilic substitution to the total synthesis of dl-physostigmine.
2003-08-08
A solid-state nitrogen-15 NMR and ab initio study of nitrobenzenes.
2003-05-30
Longevity of granular iron in groundwater treatment processes: solution composition effects on reduction of organohalides and nitroaromatic compounds.
2003-03-15
Toxicokinetics and biotransformation of p-nitrophenol in red abalone (Haliotis rufescens).
2003-02-26
Essential requirements for substrate binding affinity and selectivity toward human CYP2 family enzymes.
2003-01-01
Temperature-sensitive photochemical aromatic substitution on 4-nitroanisole.
2002-12
Controlled release of 4-nitroanisole from poly(lactic acid) nanoparticles.
2002-07-18
Molecular rulers: new families of molecules for measuring interfacial widths.
2002-05-01
Evidence for singlet oxygen involvement in rat and human cytochrome P450-dependent substrate oxidations.
2002
Factors affecting mass transfer limited biodegradation in saturated porous media.
2001-07
Binding and oxidation of alkyl 4-nitrophenyl ethers by rabbit cytochrome P450 1A2: evidence for two binding sites.
2001-06-19
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:07 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:07 GMT 2025
Record UNII
G989Z7WOLH
Record Status Validated (UNII)
Record Version
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Name Type Language
NSC-5507
Preferred Name English
P-NITROANISOLE
MI  
Common Name English
P-NITROBENZENE METHYL ETHER
Common Name English
METHYL 4-NITROPHENYL ETHER
Systematic Name English
NITROANISOLE, P-
Common Name English
ANISOLE, P-NITRO-
Common Name English
1-METHOXY-4-NITROBENZENE
Systematic Name English
P-NITROMETHOXYBENZENE
Common Name English
4-METHOXYNITROBENZENE
Systematic Name English
4-METHOXY-1-NITROBENZENE
Systematic Name English
P-NITROANISOLE [MI]
Common Name English
4-NITROANISOLE
Systematic Name English
METHYL P-NITROPHENYL ETHER
Common Name English
4-NITROMETHOXYBENZENE
Systematic Name English
4-NITROPHENYL METHYL ETHER
Systematic Name English
4-NITRO-1-METHOXYBENZENE
Systematic Name English
P-METHOXYNITROBENZENE
Common Name English
Code System Code Type Description
CHEBI
1911
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
PUBCHEM
7485
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
MERCK INDEX
m7941
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY Merck Index
EPA CompTox
DTXSID9059208
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
202-825-3
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
CAS
100-17-4
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
NSC
5507
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
FDA UNII
G989Z7WOLH
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY
MESH
C005306
Created by admin on Mon Mar 31 18:34:07 GMT 2025 , Edited by admin on Mon Mar 31 18:34:07 GMT 2025
PRIMARY