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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 M-NITROBENZYL ALCOHOL

SMILES

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

InChI

InChIKey=CWNPOQFCIIFQDM-UHFFFAOYSA-N
InChI=1S/C7H7NO3/c9-5-6-2-1-3-7(4-6)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
Supercharged protein and peptide ions formed by electrospray ionization.
2001 Apr 1
Diastereoselective formation of host-guest complexes between a series of phosphate-bridged cavitands and alkyl- and arylammonium ions studied by liquid secondary-ion mass spectrometry.
2001 May 4
Hydrolysis of phosphotriesters: determination of transition states in parallel reactions by heavy-atom isotope effects.
2001 Sep 26
The importance of preferential solvation of the CN ligands in electron- and proton-transfers observed for cis-[Ru(CN)2(bpy)2] under ion bombardment.
2002 Oct
Matrix addition by condensation for matrix-assisted laser desorption/ionization of collected aerosol particles.
2002 Sep 15
Mechanism of charging and supercharging molecules in electrospray ionization.
2003 Feb 26
Collisionally activated dissociation of supercharged proteins formed by electrospray ionization.
2003 Sep 1
On-line laser desorption/ionization mass spectrometry of matrix-coated aerosols.
2004
Electron ionisation and fast-atom bombardment mass spectrometry study of diaryl carbonates.
2006
Studies on high-energy collision-induced dissociation of endogenous cannabinoids: 2-arachidonoylglycerol and n-arachidonoylethanolamide in FAB-mass spectrometry.
2006 Jul
Structural determination of monoacylglycerols extracted from marine sponge by fast atom bombardment tandem mass spectrometry.
2007
Peptide sequencing and characterization of post-translational modifications by enhanced ion-charging and liquid chromatography electron-transfer dissociation tandem mass spectrometry.
2007 Dec 15
Synthesis, characterization, and in vitro cytotoxic activities of benzaldehyde thiosemicarbazone derivatives and their palladium (II) and platinum (II) complexes against various human tumor cell lines.
2008
FAB mass spectrometry of Au25(SR)18 nanoparticles.
2008 Sep 15
Reactive-electrospray-assisted laser desorption/ionization for characterization of peptides and proteins.
2008 Sep 15
Identification of 2-aminothiazole-4-carboxylate derivatives active against Mycobacterium tuberculosis H37Rv and the beta-ketoacyl-ACP synthase mtFabH.
2009
Increasing charge while preserving noncovalent protein complexes for ESI-MS.
2009 Apr
Direct screening of chiral discrimination abilities of chiral hosts using mass spectrometry.
2009 Feb
Comparison of infrared multiphoton dissociation and collision-induced dissociation of supercharged peptides in ion traps.
2009 Mar
Origin of supercharging in electrospray ionization of noncovalent complexes from aqueous solution.
2009 Oct
Application of spectroscopic methods for structural analysis of chitin and chitosan.
2010 Apr 29
New reagents for increasing ESI multiple charging of proteins and protein complexes.
2010 Jan
Evaporation and discharge dynamics of highly charged multicomponent droplets generated by electrospray ionization.
2010 Jan 28
Effects of supercharging reagents on noncovalent complex structure in electrospray ionization from aqueous solutions.
2010 Oct
New reagents for enhanced liquid chromatographic separation and charging of intact protein ions for electrospray ionization mass spectrometry.
2010 Sep 1
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:27:19 UTC 2023
Edited
by admin
on Fri Dec 15 17:27:19 UTC 2023
Record UNII
F829X990IV
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
M-NITROBENZYL ALCOHOL
Systematic Name English
NSC-5388
Code English
NITROBENZYL ALCOHOL, 3-
Systematic Name English
M-NITROPHENYLMETHANOL
Systematic Name English
M-(HYDROXYMETHYL)NITROBENZENE
Systematic Name English
3-NITROBENZENEMETHANOL
Systematic Name English
BENZYL ALCOHOL, M-NITRO-
Systematic Name English
BENZENEMETHANOL, 3-NITRO-
Systematic Name English
3-NITROBENZYL ALCOHOL
Systematic Name English
(3-NITROPHENYL)METHANOL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID0060698
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY
NSC
5388
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY
PUBCHEM
69267
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY
ECHA (EC/EINECS)
210-588-2
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY
CAS
619-25-0
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY
FDA UNII
F829X990IV
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY
WIKIPEDIA
3-Nitrobenzyl alcohol
Created by admin on Fri Dec 15 17:27:19 UTC 2023 , Edited by admin on Fri Dec 15 17:27:19 UTC 2023
PRIMARY