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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-NITROBENZYL ALCOHOL

SMILES

OCC1=CC=C(C=C1)[N+]([O-])=O

InChI

InChIKey=JKTYGPATCNUWKN-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c9-5-6-1-3-7(4-2-6)8(10)11/h1-4,9H,5H2

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
Supercritical carbon dioxide, a new medium for aerobic alcohol oxidations catalysed by copper-TEMPO.
2010-01-21
Isolation and characterization of a 4-nitrotoluene-oxidizing enzyme from activated sludge by a metagenomic approach.
2010
4-Nitro-benzyl 2-bromo-acetate.
2009-06-06
Mitigating unwanted photophysical processes for improved single-molecule fluorescence imaging.
2009-03-18
Fluorocarbon soluble copper(II) carboxylate complexes with nonfluoroponytailed nitrogen ligands as precatalysts for the oxidation of alkenols and alcohols under fluorous biphasic or thermomorphic modes: structural and mechanistic aspects.
2005-12-26
Fungal cytochrome P450s catalyzing hydroxylation of substituted toluenes to form their hydroxymethyl derivatives.
2004-05-15
Fluorous biphasic catalysis: synthesis and characterization of copper(I) and copper(II) fluoroponytailed 1,4,7-Rf-TACN and 2,2'-Rf-bipyridine complexes--their catalytic activity in the oxidation of hydrocarbons, olefins, and alcohols, including mechanistic implications.
2003-09-05
Glycosylation of sialyl acetates with a novel catalyst combination: bismuth triflate and BF3.OEt2 system.
2003-07-17
Micellar electrokinetic chromatography with on-line Fourier transform infrared detection.
2003-02
Catalytic reaction profile for alcohol oxidation by galactose oxidase.
2001-06-19
X-ray structures of a hydrolytic antibody and of complexes elucidate catalytic pathway from substrate binding and transition state stabilization through water attack and product release.
1997-07-22
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:34:08 GMT 2025
Edited
by admin
on Mon Mar 31 18:34:08 GMT 2025
Record UNII
86BTJ68Y9M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-NITROBENZYL ALCOHOL
Common Name English
NSC-5389
Preferred Name English
P-NITROPHENYLMETHANOL
Common Name English
(4-NITROPHENYL)METHANOL
Systematic Name English
BENZENEMETHANOL, 4-NITRO-
Systematic Name English
4-(HYDROXYMETHYL)NITROBENZENE
Systematic Name English
1-(HYDROXYMETHYL)-4-NITROBENZENE
Systematic Name English
4-NITROBENZENEMETHANOL
Systematic Name English
4-NITROBENZYL ALCOHOL
Systematic Name English
NITROBENZYL ALCOHOL, 4-
Systematic Name English
BENZYL ALCOHOL, P-NITRO-
Systematic Name English
P-(HYDROXYMETHYL)NITROBENZENE
Common Name English
Code System Code Type Description
PUBCHEM
69275
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY
NSC
5389
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY
CAS
619-73-8
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY
EPA CompTox
DTXSID1052298
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY
FDA UNII
86BTJ68Y9M
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY
CHEBI
41214
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY
ECHA (EC/EINECS)
210-611-6
Created by admin on Mon Mar 31 18:34:08 GMT 2025 , Edited by admin on Mon Mar 31 18:34:08 GMT 2025
PRIMARY