Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C6H6N2O3 |
| Molecular Weight | 154.1234 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
NC1=CC(=CC=C1O)[N+]([O-])=O
InChI
InChIKey=VLZVIIYRNMWPSN-UHFFFAOYSA-N
InChI=1S/C6H6N2O3/c7-5-3-4(8(10)11)1-2-6(5)9/h1-3,9H,7H2
| Molecular Formula | C6H6N2O3 |
| Molecular Weight | 154.1234 |
| Charge | 0 |
| Count |
|
| Stereochemistry | ACHIRAL |
| Additional Stereochemistry | No |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Optical Activity | NONE |
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Initiation and inhibition of free radical processes in H2O2-metmyoglobin (methemoglobin)-2,2'-azino-bis-(3-ethylbenzthiazoline-6-sulfonic acid) systems. | 2001 May |
|
| Peroxidase-catalyzed co-oxidation of 3,3',5,5'-tetramethylbenzidine in the presence of substituted phenols and their polydisulfides. | 2004 Jan |
|
| Synthesis, anti-inflammatory and analgesic activities evaluation of some mono, bi and tricyclic pyrimidine derivatives. | 2005 Nov 15 |
|
| LC-MS-MS analysis of 2,4-dinitrophenol and its phase I and II metabolites in a case of fatal poisoning. | 2007 Jan-Feb |
|
| (E)-2-[(2-Hydr-oxy-5-nitro-phen-yl)iminiometh-yl]phenolate. | 2009 Feb 11 |
|
| (E)-2-[(2-Hydr-oxy-5-nitro-phen-yl)iminiometh-yl]-4-nitro-phenolate. | 2009 Jan 14 |
|
| Final report on the safety assessment of amino nitrophenols as used in hair dyes. | 2009 Nov-Dec |
|
| 2-Amino-4-nitro-phenol monohydrate. | 2010 Sep 11 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Sat Dec 16 01:07:12 GMT 2023
by
admin
on
Sat Dec 16 01:07:12 GMT 2023
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| Record UNII |
G501UCI6T9
|
| Record Status |
Validated (UNII)
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| Record Version |
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3613389
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