Details
| Stereochemistry | ACHIRAL |
| Molecular Formula | C4H5N3O2 |
| Molecular Weight | 127.1014 |
| Optical Activity | NONE |
| Defined Stereocenters | 0 / 0 |
| E/Z Centers | 0 |
| Charge | 0 |
SHOW SMILES / InChI
SMILES
CC1=NC(=CN1)[N+]([O-])=O
InChI
InChIKey=FFYTTYVSDVWNMY-UHFFFAOYSA-N
InChI=1S/C4H5N3O2/c1-3-5-2-4(6-3)7(8)9/h2H,1H3,(H,5,6)
| Molecular Formula | C4H5N3O2 |
| Molecular Weight | 127.1014 |
| 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 |
|---|---|---|
| Ethyl 2-(2-methyl-4-nitro-1H-imidazol-1-yl)acetate. | 2010-09-25 |
|
| The application of resonance light scattering technique for the determination of tinidazole in drugs. | 2007 |
|
| Evaluation of 99mTc(CO)3 complex of 2-methyl-5-nitroimidazole as an agent for targeting tumor hypoxia. | 2006-12-01 |
|
| Radiosynthesis and evaluation of two novel 123I-labeled 2-methyl-4-nitroimidazole derivatives as potential infection imaging agents. | 2005-05 |
|
| [Synthesis and antibacterial activity of ciprofloxacin derivatives]. | 2005-02 |
|
| Synthesis and anti-tuberculosis activity of N-aryl-C-nitroazoles. | 2004-10 |
|
| The effects of the substitution on the imidazole ligand on the photochemical properties of fac-[Mn(CO)3(phen)(Imidazole)](SO3CF3) complexes. | 2004-07-14 |
|
| Effect of the leaving group on the electrodic reduction mechanism of anti-Helicobacter pylori metronidazole derivatives, in aprotic and protic media. | 2004-06 |
|
| Michael addition of imidazole with acrylates catalyzed by alkaline protease from Bacillus subtilis in organic media. | 2004-03 |
|
| Synthesis of N-alkylated derivatives of imidazole as antibacterial agents. | 2003-09-01 |
|
| [Synthesis and antibacterial activity of pyridonecarboxylic acid derivatives containing 2-methyl-5-nitroimidazol]. | 2003-04 |
| Substance Class |
Chemical
Created
by
admin
on
Edited
Mon Mar 31 18:59:35 GMT 2025
by
admin
on
Mon Mar 31 18:59:35 GMT 2025
|
| Record UNII |
24AG2WW15W
|
| Record Status |
Validated (UNII)
|
| Record Version |
|
-
Download
| Name | Type | Language | ||
|---|---|---|---|---|
|
Preferred Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Common Name | English | ||
|
Systematic Name | English | ||
|
Systematic Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Common Name | English | ||
|
Code | English | ||
|
Systematic Name | English |
| Code System | Code | Type | Description | ||
|---|---|---|---|---|---|
|
12760
Created by
admin on Mon Mar 31 18:59:35 GMT 2025 , Edited by admin on Mon Mar 31 18:59:35 GMT 2025
|
PRIMARY | |||
|
211-790-3
Created by
admin on Mon Mar 31 18:59:35 GMT 2025 , Edited by admin on Mon Mar 31 18:59:35 GMT 2025
|
PRIMARY | |||
|
696-23-1
Created by
admin on Mon Mar 31 18:59:35 GMT 2025 , Edited by admin on Mon Mar 31 18:59:35 GMT 2025
|
PRIMARY | |||
|
1667530
Created by
admin on Mon Mar 31 18:59:35 GMT 2025 , Edited by admin on Mon Mar 31 18:59:35 GMT 2025
|
PRIMARY | |||
|
24AG2WW15W
Created by
admin on Mon Mar 31 18:59:35 GMT 2025 , Edited by admin on Mon Mar 31 18:59:35 GMT 2025
|
PRIMARY | |||
|
DTXSID2061010
Created by
admin on Mon Mar 31 18:59:35 GMT 2025 , Edited by admin on Mon Mar 31 18:59:35 GMT 2025
|
PRIMARY |
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> METABOLITE |
URINE
|
| Related Record | Type | Details | ||
|---|---|---|---|---|
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
Ph.Eur.; USP
|
||
|
PARENT -> IMPURITY |
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
|
