Ethyl 1H-1,2,4-triazole-5-carboxylate, with the CAS number 64922-04-9, is a chemical compound characterized by its triazole ring structure, which is a five-membered heterocyclic compound containing three nitrogen atoms. This substance typically appears as a white to off-white solid and is soluble in polar organic solvents. It is known for its role in various chemical reactions, particularly in the synthesis of agrochemicals and pharmaceuticals, due to its ability to act as a building block for more complex molecules. The presence of the carboxylate group enhances its reactivity, making it a useful intermediate in organic synthesis. Additionally, the ethyl ester functionality contributes to its solubility and reactivity profile. Ethyl 1H-1,2,4-triazole-5-carboxylate may exhibit biological activity, which has led to interest in its potential applications in medicinal chemistry. As with many chemical substances, handling should be done with care, following appropriate safety protocols to mitigate any risks associated with its use.

ethyl 1H-1,2,4-triazole-5-carboxylate

64922-04-9: 1H-1,2,4-triazole-3-carboxylic acid, ethyl ester, Ethyl 1H-1,2,4-Triazole-3-Carboxylate

1H-[1,2,4]Triazole-3-carboxylic acid, ethyl ester

Ethyl-1H-1,2,4-triazole-5-carboxylate belongs to the class of triazole derivatives. It can be used as a catalyst for the cyclocondensation of terminal alkyne and aldehyde. The reaction is initiated by catalytic amounts of transition metal ions (e.g., Fe3+). Ethyl-1H-1,2,4-triazole-5-carboxylate also catalyses the formation of amide bonds in organic synthesis reactions. The compound has been shown to cleave DNA at antigenomic sites with an efficiency that is comparable to that of hydroxylamine.

CAS 64922-04-9: ethyl 1H-1,2,4-triazole-5-carboxylate

1H-[1,2,4]Triazole-3-carboxylic acid, ethyl ester

Ref: IN-DA00EJUT

Ethyl-1H-1,2,4-triazole-5-carboxylate

Ref: 3D-FE166551

Ethyl 1H-1,2,4-triazole-5-carboxylate

Ref: 10-F385865