Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C7H6N2O5 |
| Molecular Weight | 198.1329 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
COC1=C(C=C(C=C1)[N+]([O-])=O)[N+]([O-])=O
InChI
InChIKey=CVYZVNVPQRKDLW-UHFFFAOYSA-N
InChI=1S/C7H6N2O5/c1-14-7-3-2-5(8(10)11)4-6(7)9(12)13/h2-4H,1H3
| Molecular Formula | C7H6N2O5 |
| Molecular Weight | 198.1329 |
| 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 |
|---|---|---|
| Biological transformation pathways of 2,4-dinitro anisole and N-methyl paranitro aniline in anaerobic fluidized-bed bioreactors. | 2010-11 |
|
| One-electron standard reduction potentials of nitroaromatic and cyclic nitramine explosives. | 2010-10 |
|
| Stability of nitroaromatic specialty explosives in reversed-phase liquid chromatographic systems. | 2009-03-15 |
|
| Equilibrium and column adsorption studies of 2,4-dinitroanisole (DNAN) on surface modified granular activated carbons. | 2009-02 |
|
| Analysis of bacterial community diversity in anaerobic fluidized bed bioreactors treating 2,4-dinitroanisole (DNAN) and n-methyl-4-nitroaniline (MNA) using 16S rRNA gene clone libraries. | 2009 |
Patents
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 17:51:34 GMT 2025
by
admin
on
Mon Mar 31 17:51:34 GMT 2025
|
| Record UNII |
1L0OD70295
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Systematic Name | English | ||
|
Preferred Name | English | ||
|
Systematic Name | English |
| Classification Tree | Code System | Code | ||
|---|---|---|---|---|
|
EPA PESTICIDE CODE |
37503
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
||
|
NCI_THESAURUS |
C737
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
8733
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
84559
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
C539360
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
8385
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
204-310-9
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
C83511
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
1L0OD70295
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
119-27-7
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
DTXSID9041366
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY | |||
|
2,4-Dinitroanisole
Created by
admin on Mon Mar 31 17:51:34 GMT 2025 , Edited by admin on Mon Mar 31 17:51:34 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
|
ACTIVE MOIETY |