2-Pyrrolidin-1-ylpropanoic acid, also known by its CAS number 123912-78-7, is an organic compound characterized by the presence of a pyrrolidine ring and a propanoic acid moiety. This substance features a five-membered nitrogen-containing heterocycle, which contributes to its unique chemical properties, including potential basicity due to the nitrogen atom. The propanoic acid group imparts acidic characteristics, allowing it to participate in various chemical reactions, such as esterification and amidation. 2-Pyrrolidin-1-ylpropanoic acid is often studied for its potential applications in pharmaceuticals and biochemistry, particularly in the development of compounds that can interact with biological systems. Its solubility in polar solvents, such as water and alcohols, is influenced by the functional groups present. Additionally, the compound's molecular structure may allow for specific interactions with receptors or enzymes, making it of interest in medicinal chemistry. Overall, 2-pyrrolidin-1-ylpropanoic acid exemplifies the diverse functionalities that can arise from combining cyclic and acyclic structures in organic chemistry.

2-pyrrolidin-1-ylpropanoic acid

123912-78-7: 2-Pyrrolidin-1-ylpropanoic acid, also known by its CAS number 123912-78-7, is an organic compound characterized by the presence of a pyrrolidine ring and a propanoic acid moiety. This substance features a five-membered nitrogen-containing heterocycle, which contributes to its unique chemical properties, including potential basicity due to the nitrogen atom. The propanoic acid group imparts acidic characteristics, allowing it to participate in various chemical reactions, such as esterification and amidation. 2-Pyrrolidin-1-ylpropanoic acid is often studied for its potential applications in pharmaceuticals and biochemistry, particularly in the development of compounds that can interact with biological systems. Its solubility in polar solvents, such as water and alcohols, is influenced by the functional groups present. Additionally, the compound's molecular structure may allow for specific interactions with receptors or enzymes, making it of interest in medicinal chemistry. Overall, 2-pyrrolidin-1-ylpropanoic acid exemplifies the diverse functionalities that can arise from combining cyclic and acyclic structures in organic chemistry.

CAS 123912-78-7

2-pyrrolidin-1-ylpropanoic acid

1-Pyrrolidineacetic acid, α-methyl-

Ref: IN-DA000L7U

2-(1-Pyrrolidyl)propanoic acid

Ref: 54-OR1006598

2-Pyrrolidin-1-yl-propionic acid

Ref: 10-F028342