About This Item
Produtos recomendados
Nível de qualidade
Ensaio
98%
pf
249 °C (lit.)
grupo funcional
nitro
cadeia de caracteres SMILES
Cc1[nH]cnc1[N+]([O-])=O
InChI
1S/C4H5N3O2/c1-3-4(7(8)9)6-2-5-3/h2H,1H3,(H,5,6)
chave InChI
WSYOWIMKNNMEMZ-UHFFFAOYSA-N
Descrição geral
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.
Aplicação
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).
Palavra indicadora
Warning
Frases de perigo
Declarações de precaução
Classificações de perigo
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Órgãos-alvo
Respiratory system
Código de classe de armazenamento
11 - Combustible Solids
Classe de risco de água (WGK)
WGK 3
Ponto de fulgor (°F)
Not applicable
Ponto de fulgor (°C)
Not applicable
Equipamento de proteção individual
dust mask type N95 (US), Eyeshields, Gloves
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Localized cell stimulation by nitric oxide using a photoactive porous coordination polymer platform.
Nature communications, 4, 2684-2684 (2013-10-26)
Functional cellular substrates for localized cell stimulation by small molecules provide an opportunity to control and monitor cell signalling networks chemically in time and space. However, despite improvements in the controlled delivery of bioactive compounds, the precise localization of gaseous
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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