The chemical substance known as "(3S,4R)-1-(tert-butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid" is a pyrrolidine derivative characterized by its specific stereochemistry, indicated by the (3S,4R) configuration. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during reactions. The presence of a 4-methoxyphenyl group suggests that it may exhibit aromatic characteristics, potentially influencing its reactivity and solubility. As a carboxylic acid, it possesses acidic properties, allowing it to participate in various chemical reactions, such as esterification or amidation. The compound's structure indicates potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, the specific stereochemistry may play a crucial role in its biological activity and pharmacokinetics. Overall, this compound represents a versatile building block in organic synthesis and drug development.

(3S,4R)-1-(tert-butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylicacid

1269260-00-5: The chemical substance known as "(3S,4R)-1-(tert-butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid" is a pyrrolidine derivative characterized by its specific stereochemistry, indicated by the (3S,4R) configuration. This compound features a tert-butoxycarbonyl (Boc) protecting group, which is commonly used in organic synthesis to protect amines during reactions. The presence of a 4-methoxyphenyl group suggests that it may exhibit aromatic characteristics, potentially influencing its reactivity and solubility. As a carboxylic acid, it possesses acidic properties, allowing it to participate in various chemical reactions, such as esterification or amidation. The compound's structure indicates potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Additionally, the specific stereochemistry may play a crucial role in its biological activity and pharmacokinetics. Overall, this compound represents a versatile building block in organic synthesis and drug development.

CAS 1269260-00-5

(3S,4R)-1-(tert-butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylicacid

(3S,4R)-1-(tert-Butoxycarbonyl)-4-(4-methoxyphenyl)pyrrolidine-3-carboxylic acid

Ref: IN-DA000THE