(2S,4S)-4-aminopyrrolidine-2-carboxylic acid dihydrochloride
$325.00
CAS No.: 16257-84-4
Catalog No.: 192997
Purity: 95%
MF: C5H12Cl2N2O2
MW: 203.069
Storage: 2-8 degree Celsius
SMILES: Cl.Cl.N[C@H]1C[C@H](NC1)C(=O)O
Catalog No.: 192997
Purity: 95%
MF: C5H12Cl2N2O2
MW: 203.069
Storage: 2-8 degree Celsius
SMILES: Cl.Cl.N[C@H]1C[C@H](NC1)C(=O)O
(2S,4S)-4-aminopyrrolidine-2-carboxylic acid dihydrochloride; CAS No.: 16257-84-4; (2S,4S)-4-aminopyrrolidine-2-carboxylic acid dihydrochloride. PROPERTIES: This compound appears as a white to off-white crystalline solid with molecular formula C5H10N2O2 {2HCl and a molecular weight of 192.06 g/mol. It exhibits a melting point in the range of 198-202 C and shows good solubility in water and common polar solvents like methanol. The substance is hygroscopic and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at room temperature with protection from moisture and light. When handling, standard laboratory safety precautions should be observed, including the use of gloves and eye protection, as (2S,4S)-4-aminopyrrolidine-2-carboxylic acid dihydrochloride may cause skin and eye irritation. The amino group requires careful handling in strongly acidic environments. APPLICATIONS: In medicinal chemistry, (2S,4S)-4-aminopyrrolidine-2-carboxylic acid dihydrochloride serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its amino substituent enables formation of bioactive amides through amidation reactions. Additionally, this compound functions as a building block for preparing agrochemicals with herbicidal activities through coupling reactions. Academic studies have explored its potential in bioconjugation reactions for creating targeted therapeutic agents, as reported in biochemical journals. The pyrrolidine ring system also facilitates coordination with metal ions, making it valuable for creating coordination polymers in materials science applications, as evidenced by structural chemistry publications.
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