Details
Stereochemistry | ACHIRAL |
Molecular Formula | C7H3ClN2O5 |
Molecular Weight | 230.562 |
Optical Activity | NONE |
Defined Stereocenters | 0 / 0 |
E/Z Centers | 0 |
Charge | 0 |
SHOW SMILES / InChI
SMILES
[O-][N+](=O)C1=CC(=CC(=C1)C(Cl)=O)[N+]([O-])=O
InChI
InChIKey=NNOHXABAQAGKRZ-UHFFFAOYSA-N
InChI=1S/C7H3ClN2O5/c8-7(11)4-1-5(9(12)13)3-6(2-4)10(14)15/h1-3H
Molecular Formula | C7H3ClN2O5 |
Molecular Weight | 230.562 |
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 |
---|---|---|
A Fourier-transform ion cyclotron resonance study of the 3,5-didehydrophenyl cation. | 2001 Mar |
|
Sensitive determination of methylenedioxylated amphetamines by liquid chromatography. | 2001 May |
|
Determination of aliphatic amines in water by liquid chromatography using solid-phase extraction cartridges for preconcentration and derivatization. | 2001 Oct |
|
Isolation of poly(propylene glycol)s from water for quantitative analysis by reversed-phase liquid chromatography. | 2003 Dec 22 |
|
[Synthesis of a novel starch derivative and its adsorption property for creatinine]. | 2003 Mar |
|
Analysis of neutral surfactants by non-aqueous capillary electrophoresis using an electroosmotic flow reversal. | 2005 Mar 11 |
|
Optimization of HPLC chromatographic conditions for determination of Transkarbam 12 and its degradation products. | 2006 Sep 11 |
|
Pi-Pi complexation of bupivacaine and analogues with aromatic receptors: implications for overdose remediation. | 2007 |
|
Lower-rim substituted calixarenes and their applications. | 2007 |
|
Imprinted nanoporous organosilicas for selective adsorption of nitroenergetic targets. | 2008 Aug 19 |
|
Preparation and adsorption characteristic of polymeric microsphere with strong adsorbability for creatinine. | 2008 May-Jun |
|
3,5-Dinitro-benzoyl chloride. | 2009 Sep 12 |
|
Chemical stability of 4'-azidocytidine and its prodrug balapiravir. | 2010 Apr |
Substance Class |
Chemical
Created
by
admin
on
Edited
Fri Dec 15 18:50:37 GMT 2023
by
admin
on
Fri Dec 15 18:50:37 GMT 2023
|
Record UNII |
5JFA2DVM4D
|
Record Status |
Validated (UNII)
|
Record Version |
|
-
Download
Name | Type | Language | ||
---|---|---|---|---|
|
Systematic Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English |
Code System | Code | Type | Description | ||
---|---|---|---|---|---|
|
DTXSID2059194
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
C013964
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
202-750-6
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
99-33-2
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
7432
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
5JFA2DVM4D
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
2697
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
3,5-Dinitrobenzoyl chloride
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | |||
|
m4573
Created by
admin on Fri Dec 15 18:50:37 GMT 2023 , Edited by admin on Fri Dec 15 18:50:37 GMT 2023
|
PRIMARY | Merck Index |