CAS 40648-96-2

1-Methyl-4-nitro-1H-imidazole-5-carbonitrile

Description:

1-Methyl-4-nitro-1H-imidazole-5-carbonitrile, with the CAS number 40648-96-2, is a heterocyclic organic compound characterized by its imidazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a methyl group and a nitro group, contributing to its unique chemical properties. The presence of the carbonitrile functional group enhances its reactivity and potential applications in various chemical reactions. Typically, compounds like this are of interest in medicinal chemistry and material science due to their biological activity and ability to form coordination complexes. The nitro group can serve as a site for further chemical modifications, while the carbonitrile group can participate in nucleophilic reactions. Additionally, the compound's solubility and stability can vary depending on the solvent and environmental conditions, making it important to consider these factors in practical applications. Overall, 1-Methyl-4-nitro-1H-imidazole-5-carbonitrile is a versatile compound with potential uses in pharmaceuticals and agrochemicals.

Formula: C₅H₄N₄O₂

InChI: InChI=1S/C5H4N4O2/c1-8-3-7-5(9(10)11)4(8)2-6/h3H,1H3

InChI key: InChIKey=LXXDMPXVEZYDCI-UHFFFAOYSA-N

SMILES: C(#N)C1=C(N(=O)=O)N=CN1C

Synonyms:

• 1-Methyl-4-nitro-5-cyanoimidazole
• 1-Methyl-4-nitroimidazole-5-carbonitrile
• 1H-imidazole-5-carbonitrile, 1-methyl-4-nitro-
• 3-Methyl-5-nitro-3H-imidazole-4-carbonitrile
• 3-Methyl-5-nitroimidazole-4-carbonitrile
• 5-Cyano-1-methyl-4-nitroimidazole
• Imidazole-5-carbonitrile, 1-methyl-4-nitro-
• NSC 43810
• NSC 7854
• 1-Methyl-4-nitro-1H-imidazole-5-carbonitrile

1-METHYL-4-NITRO-1H-IMIDAZOLE-5-CARBONITRILE

CAS: 40648-96-2

Formula: C₅H₄N₄O₂

Purity: 95.0%

Molecular weight: 152.113

Ref: 10-F331722

1-Methyl-4-nitro-1H-imidazole-5-carbonitrile

CAS: 40648-96-2

1-Methyl-4-nitro-1H-imidazole-5-carbonitrile is a nitroimidazole that is activated by oxidation. It has been shown to be effective against strains of bacteria that are resistant to other antibiotics, such as methicillin and erythromycin. Nitroimidazoles are analogues of sulfonamides and have a reactive methylsulfonyl group that can be used to form covalent bonds with nucleophiles. 1-Methyl-4-nitro-1H-imidazole-5-carbonitrile is an example of a substituent in which the substituent is a bromo group. This substituent has been shown to react with nucleophiles, such as alkyl halides and thiols, which may lead to the formation of new compounds.

Formula: C₅H₄N₄O₂

Purity: Min. 95%

Molecular weight: 152.11 g/mol

Ref: 3D-QBA64896