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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
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 Jul 22
Micellar electrokinetic chromatography with on-line Fourier transform infrared detection.
2003 Feb
Glycosylation of sialyl acetates with a novel catalyst combination: bismuth triflate and BF3.OEt2 system.
2003 Jul 17
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 Sep 5
Fungal cytochrome P450s catalyzing hydroxylation of substituted toluenes to form their hydroxymethyl derivatives.
2004 May 15
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 Dec 26
4-Nitro-benzyl 2-bromo-acetate.
2009 Jun 6
Mitigating unwanted photophysical processes for improved single-molecule fluorescence imaging.
2009 Mar 18
Isolation and characterization of a 4-nitrotoluene-oxidizing enzyme from activated sludge by a metagenomic approach.
2010
Supercritical carbon dioxide, a new medium for aerobic alcohol oxidations catalysed by copper-TEMPO.
2010 Jan 21
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:40:08 GMT 2023
Edited
by admin
on Fri Dec 15 16:40:08 GMT 2023
Record UNII
86BTJ68Y9M
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
P-NITROBENZYL ALCOHOL
Common Name English
P-NITROPHENYLMETHANOL
Common Name English
NSC-5389
Code 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 Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
PRIMARY
NSC
5389
Created by admin on Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
PRIMARY
CAS
619-73-8
Created by admin on Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
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EPA CompTox
DTXSID1052298
Created by admin on Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
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FDA UNII
86BTJ68Y9M
Created by admin on Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
PRIMARY
CHEBI
41214
Created by admin on Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
PRIMARY
ECHA (EC/EINECS)
210-611-6
Created by admin on Fri Dec 15 16:40:08 GMT 2023 , Edited by admin on Fri Dec 15 16:40:08 GMT 2023
PRIMARY