CAS 54828-05-6

1-methyl-4-nitro-1H-imidazole-5-carboxylic acid

Description:

1-Methyl-4-nitro-1H-imidazole-5-carboxylic acid is a heterocyclic organic compound characterized by its imidazole ring, which contains both a methyl and a nitro group as substituents. The presence of the carboxylic acid functional group contributes to its acidic properties, making it soluble in polar solvents. This compound typically exhibits a yellow to orange color due to the nitro group, which can also influence its reactivity and interaction with other chemical species. It is often used in pharmaceutical research and as an intermediate in the synthesis of various bioactive compounds. The nitro group can participate in electrophilic substitution reactions, while the carboxylic acid can engage in acid-base reactions. Additionally, the compound's structure allows for potential hydrogen bonding, which can affect its solubility and interaction with biological systems. Overall, 1-methyl-4-nitro-1H-imidazole-5-carboxylic acid is notable for its unique structural features and potential applications in medicinal chemistry.

Formula: C₅H₅N₃O₄

InChI: InChI=1/C5H5N3O4/c1-7-2-6-4(8(11)12)3(7)5(9)10/h2H,1H3,(H,9,10)

SMILES: Cn1cnc(c1C(=O)O)N(=O)=O

Synonyms:

• 1H-imidazole-5-carboxylic acid, 1-methyl-4-nitro-

1-Methyl-4-nitro-1H-imidazole-5-carboxylic Acid

Controlled Product

CAS: 54828-05-6

Applications A derivative of imidazole used in the synthesis of heteroxanthine.
References Sarasin, J., et al.: Helv. Chim. Acta, 7, 713 (1924),

Formula: C₅H₅N₃O₄

Color and Shape: Neat

Molecular weight: 171.11

Ref: TR-M323748