94489
1-Methyl-5-nitroimidazole
>97.0% (HPLC)
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About This Item
Empirical Formula (Hill Notation):
C4H5N3O2
CAS Number:
Molecular Weight:
127.10
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
221-225-2
Beilstein/REAXYS Number:
123550
MDL number:
Assay:
>97.0% (HPLC)
Form:
solid
InChI key
JLZXSFPSJJMRIX-UHFFFAOYSA-N
InChI
1S/C4H5N3O2/c1-6-3-5-2-4(6)7(8)9/h2-3H,1H3
SMILES string
Cn1cncc1[N+]([O-])=O
assay
>97.0% (HPLC)
form
solid
mp
54-57 °C
functional group
nitro
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Mónica Mendes et al.
International journal of molecular sciences, 20(24) (2019-12-11)
Electron transfer induced decomposition mechanism of nitroimidazole and a selection of analogue molecules in collisions with neutral potassium (K) atoms from 10 to 1000 eV have been thoroughly investigated. In this laboratory collision regime, the formation of negative ions was
S Pandeti et al.
The Journal of chemical physics, 150(1), 014302-014302 (2019-01-10)
Nitroimidazolic radiosensitizers are used in radiation therapy to selectively sensitize cancer cells deprived of oxygen, and the actual mechanism of radiosensitization is still not understood. Selecting five radiosensitizers (1-methyl-5-nitroimidazole, ronidazole, ornidazole, metronidazole, and nimorazole) with a common 5-nitroimidazolic ring with
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