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5-Methyl-4-nitroimidazol
98%
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About This Item
Empfohlene Produkte
Qualitätsniveau
Assay
98%
mp (Schmelzpunkt)
249 °C (lit.)
Funktionelle Gruppe
nitro
SMILES String
Cc1[nH]cnc1[N+]([O-])=O
InChI
1S/C4H5N3O2/c1-3-4(7(8)9)6-2-5-3/h2H,1H3,(H,5,6)
InChIKey
WSYOWIMKNNMEMZ-UHFFFAOYSA-N
Allgemeine Beschreibung
5-Methyl-4-nitroimidazole, an imidazole derivative, is a heterocyclic NH-acid. Its nitration in the presence of acetic anhydride/glacial acetic acid has been studied.
Anwendung
5-Methyl-4-nitroimidazole may be used in the following:
- To trap the reactive 1:1 intermediate formed during the reaction between triphenylphosphine and dibenzoylacetylene.
- As a starting reagent in the synthesis of pyrazole derivatives.
- Fabrication of zeolitic imidazolate frameworks (ZIFs).
Signalwort
Warning
H-Sätze
Gefahreneinstufungen
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Zielorgane
Respiratory system
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
Not applicable
Flammpunkt (°C)
Not applicable
Persönliche Schutzausrüstung
dust mask type N95 (US), Eyeshields, Gloves
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Reaction between heterocyclic NH-acids and dibenzoylacetylene in the presence of triphenylphosphine. Simple synthesis of 1-(3-furyl)-1H-imidazole derivatives.
Tetrahedron Letters, 43(51), 9449-9452 (2002)
Synthesis, metabolism and structure-mutagenicity relationships of novel 4-nitro-(imidazoles and pyrazoles) in Salmonella typhimurium.
Mutation Research. Fundamental and Molecular Mechanisms of Mutagenesis, 397(2), 293-301 (1998)
1, 4-Dinitroimidazole and derivatives. Structure and thermal rearrangement.
Australian Journal of Chemistry, 42(8), 1281-1289 (1989)
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