5-Chloro-3-ethyl-1-methyl-1H-pyrazole-4-carbaldehyde is a chemical compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a chloro substituent at the 5-position, an ethyl group at the 3-position, and a methyl group at the 1-position, along with an aldehyde functional group at the 4-position. The presence of the aldehyde group indicates that it can participate in various chemical reactions, such as nucleophilic addition and condensation reactions. The chloro and ethyl groups contribute to its reactivity and potential applications in organic synthesis. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests it could be used as an intermediate in the synthesis of more complex molecules. As with many organic compounds, it is important to handle it with care, considering its potential toxicity and reactivity. Proper safety protocols should be followed when working with this substance in a laboratory setting.

5-chloro-3-ethyl-1-methyl-1H-pyrazole-4-carbaldehyde

128564-56-7: 5-Chloro-3-ethyl-1-methyl-1H-pyrazole-4-carbaldehyde is a chemical compound characterized by its pyrazole ring structure, which is a five-membered ring containing two nitrogen atoms. This compound features a chloro substituent at the 5-position, an ethyl group at the 3-position, and a methyl group at the 1-position, along with an aldehyde functional group at the 4-position. The presence of the aldehyde group indicates that it can participate in various chemical reactions, such as nucleophilic addition and condensation reactions. The chloro and ethyl groups contribute to its reactivity and potential applications in organic synthesis. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests it could be used as an intermediate in the synthesis of more complex molecules. As with many organic compounds, it is important to handle it with care, considering its potential toxicity and reactivity. Proper safety protocols should be followed when working with this substance in a laboratory setting.

CAS 128564-56-7

5-chloro-3-ethyl-1-methyl-1H-pyrazole-4-carbaldehyde

5-Chloro-3-ethyl-1-methyl-1H-pyrazole-4-carbaldehyde

Ref: IN-DA000Y6N

5-Chloro-3-ethyl-1-methyl-1H-pyrazole-4-carbaldehyde

Ref: 54-OR932091

5-Chloro-3-ethyl-1-methyl-1H-pyrazole-4-carboxaldehyde

Ref: 10-F015679