4-Amino-D-proline is a non-proteinogenic amino acid characterized by its unique structure, which includes an amino group attached to the fourth carbon of the proline ring. This compound is a derivative of proline, featuring a chiral center that gives rise to its D-configuration. It is typically a white to off-white crystalline solid and is soluble in water, making it suitable for various biochemical applications. The presence of the amino group enhances its reactivity and potential for forming peptide bonds, which is significant in peptide synthesis and research. 4-Amino-D-proline is of interest in medicinal chemistry and biochemistry, particularly in studies related to protein structure and function, as well as in the development of pharmaceuticals. Its unique properties may also contribute to its role in influencing the conformation of peptides and proteins, thereby affecting their biological activity. As with many amino acids, it can participate in various chemical reactions, including acylation and alkylation, further expanding its utility in synthetic organic chemistry.

4-amino-D-proline

Applications (2R,4S)-4-Aminopyrrolidine-2-carboxylic acid dihydrochloride (cas# 263407-17-6) is a useful research chemical.


(2R,4S)-4-Aminopyrrolidine-2-carboxylic Acid dihydrochloride

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CAS 263407-17-6: 4-amino-D-proline

(2R,4S)-4-Aminopyrrolidine-2-carboxylic Acid dihydrochloride

Ref: TR-A723260

(2R,4S)-4-Aminopyrrolidine-2-carboxylic acid dihydrochloride

Ref: 3D-FA156194

D-Proline, 4-amino-, (4S)-

Ref: IN-DA002STP

(2R,4S)-4-aminopyrrolidine-2-carboxylic acid

Ref: 10-F721241

(2R,4S)-4-Aminopyrrolidine-2-carboxylic aciddihydrochloride

Ref: 10-F210517