195650
2-Nitroimidazole
98%
Synonyme(s) :
Azomycin
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A propos de cet article
Formule empirique (notation de Hill) :
C3H3N3O2
Numéro CAS:
Poids moléculaire :
113.07
UNSPSC Code:
12352005
NACRES:
NA.22
PubChem Substance ID:
EC Number:
208-425-5
Beilstein/REAXYS Number:
116444
MDL number:
Assay:
98%
Form:
solid
Service technique
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Laissez-nous vous aiderQuality Level
assay
98%
form
solid
mp
287 °C (dec.) (lit.)
functional group
nitro
SMILES string
[O-][N+](=O)c1ncc[nH]1
InChI
1S/C3H3N3O2/c7-6(8)3-4-1-2-5-3/h1-2H,(H,4,5)
InChI key
YZEUHQHUFTYLPH-UHFFFAOYSA-N
General description
2-Nitroimidazole is a natural antibiotic.
Application
2-Nitroimidazole was used in the synthesis of:
- tert-butyl 2-(2-nitro-1H-imidazol-1-yl)ethylcarbamate
- 1-(2-(tert-butyldimethylsilyloxy)ethyl)-2-nitro-1H-imidazole
- 2-fluoro-N-(2-(2-nitro-1H-imidazol-1-yl)ethyl)acetamide
- 2-(2-methyl-5-nitro-1H-imidazol-1-yl)ethyl 2-fluoroacetate
- radiolabeling precursors - the bromo substituted analogs
- nitroimidazole substituted boronic acids, precursors for imaging hypoxic tissue
- potential site-selective radiosensitizers for estrogen receptor-rich tumors
Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Analysis Note
solubility :
50 mg/mL in NH4OH : soluble, clear, green-yellow, to very dark green-yellow to very dark yellow
50 mg/mL in NH4OH : soluble, clear, green-yellow, to very dark green-yellow to very dark yellow
signalword
Warning
hcodes
pcodes
Hazard Classifications
Acute Tox. 4 Oral
Classe de stockage
6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
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Alane Beatriz Vermelho et al.
Journal of enzyme inhibition and medicinal chemistry, 33(1), 139-146 (2017-12-02)
Sulfonamide carbonic anhydrase (CA, EC 4.2.1.1) inhibitors targeting the α-class enzyme from the protozoan pathogen Trypanosoma cruzi, responsible of Chagas disease, were recently reported. Although many such derivatives showed low nanomolar activity in vitro, they were inefficient anti-T. cruzi agents
Kazuki Yoshihara et al.
Chembiochem : a European journal of chemical biology, 18(16), 1650-1658 (2017-05-16)
The use of DNA aggregates could be a promising strategy for the molecular imaging of biological functions. Herein, phosphorescent oligodeoxynucleotides were designed with the aim of visualizing oxygen fluctuation in tumor cells. DNA-ruthenium conjugates (DRCs) that consisted of oligodeoxynucleotides, a
J. Chem. Res. Synop., 92-92 (1993)
Numéro d'article de commerce international
| Référence | GTIN |
|---|---|
| 195650-250MG | 04061838761712 |
| 195650-1G | 04061838761705 |