6-Ethyl-3-pyridinamine, with the CAS number 126553-00-2, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features an ethyl group attached to the sixth carbon of the pyridine ring and an amino group (-NH2) at the third position. The presence of the amino group makes it a primary amine, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The ethyl substituent contributes to its hydrophobic character, influencing its solubility and reactivity. 6-Ethyl-3-pyridinamine may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its properties, such as melting point, boiling point, and solubility, can vary based on environmental conditions and the presence of other functional groups. As with many nitrogen-containing heterocycles, it may also engage in hydrogen bonding, affecting its interactions with other molecules. Safety data and handling precautions should be consulted when working with this compound in a laboratory setting.

6-Ethyl-3-pyridinamine

126553-00-2: 6-Ethyl-3-pyridinamine, with the CAS number 126553-00-2, is an organic compound characterized by its pyridine ring structure, which is a six-membered aromatic ring containing one nitrogen atom. This compound features an ethyl group attached to the sixth carbon of the pyridine ring and an amino group (-NH2) at the third position. The presence of the amino group makes it a primary amine, which can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. The ethyl substituent contributes to its hydrophobic character, influencing its solubility and reactivity. 6-Ethyl-3-pyridinamine may exhibit biological activity, making it of interest in medicinal chemistry and drug development. Its properties, such as melting point, boiling point, and solubility, can vary based on environmental conditions and the presence of other functional groups. As with many nitrogen-containing heterocycles, it may also engage in hydrogen bonding, affecting its interactions with other molecules. Safety data and handling precautions should be consulted when working with this compound in a laboratory setting.

CAS 126553-00-2

6-Ethyl-3-pyridinamine

3-Pyridinamine, 6-ethyl-

Ref: IN-DA000SXA

6-Ethylpyridin-3-amine

Ref: 54-OR957164

6-Ethylpyridin-3-amine

Ref: 10-F208700