The chemical substance known as "(3R,4S)-1-tert-butoxycarbonyl-4-(3-nitrophenyl)pyrrolidine-3-carboxylic acid" is a pyrrolidine derivative characterized by its specific stereochemistry, indicated by the (3R,4S) 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 3-nitrophenyl group suggests that the compound may exhibit interesting electronic properties and potential reactivity due to the nitro substituent, which can influence both the acidity and nucleophilicity of the molecule. 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 suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Overall, this compound exemplifies the complexity and versatility of organic molecules in synthetic chemistry.

(3R,4S)-1-tert-butoxycarbonyl-4-(3-nitrophenyl)pyrrolidine-3-carboxylic acid

959577-50-5: The chemical substance known as "(3R,4S)-1-tert-butoxycarbonyl-4-(3-nitrophenyl)pyrrolidine-3-carboxylic acid" is a pyrrolidine derivative characterized by its specific stereochemistry, indicated by the (3R,4S) 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 3-nitrophenyl group suggests that the compound may exhibit interesting electronic properties and potential reactivity due to the nitro substituent, which can influence both the acidity and nucleophilicity of the molecule. 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 suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals, due to its ability to interact with biological targets. Overall, this compound exemplifies the complexity and versatility of organic molecules in synthetic chemistry.

CAS 959577-50-5

(3R,4S)-1-tert-butoxycarbonyl-4-(3-nitrophenyl)pyrrolidine-3-carboxylic acid

Boc-(+/-)-trans-4-(3-nitro-phenyl)-pyrrolidine-3-carboxylic acid

Ref: IN-DA00IJLW

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

Ref: 10-F243395