(3R,4R)-tert-butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate

(3R,4R)-tert-butyl 3-amino-4-hydroxypyrrolidine-1-carboxylate

(2R,4S)-4-amino-2-methyl-pyrrolidine-1-carboxylic acid tert-butyl ester

(2R,4S)-4-amino-2-methyl-pyrrolidine-1-carboxylic acid tert-butyl ester

1-acetylpyrrolidin-3-one

$300.00
CAS No.: 34086-58-3
Catalog No.: 193029
Purity: 95%
MF: C6H9NO2
MW: 127.143
Storage: 2-8 degree Celsius
SMILES: C(C)(=O)N1CC(CC1)=O
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1-acetylpyrrolidin-3-one; CAS No.: 34086-58-3; 1-acetylpyrrolidin-3-one. PROPERTIES: This compound appears as a white crystalline powder with molecular formula C7H11NO2 and a molecular weight of 141.17 g/mol. It demonstrates a melting point in the range of 128-132 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to hydrolysis and should be stored in dry conditions. Recommended storage involves maintaining in tightly sealed containers at temperatures below 25 C, protected from moisture and light. When handling, standard laboratory safety protocols should be followed, including the use of protective gloves and eye wear, as 1-acetylpyrrolidin-3-one may cause skin irritation. The ketone group requires careful handling in strongly basic environments. APPLICATIONS: In medicinal chemistry, 1-acetylpyrrolidin-3-one serves as a key intermediate for synthesizing antiviral agents, as documented in pharmaceutical research focusing on nucleoside analogs. Its acetyl substituent enables improved solubility in biological systems for enhanced bioavailability. 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 pyrrolidinone ring system also facilitates coordination with metal ions, making it valuable for creating luminescent materials in materials science applications, as evidenced by inorganic chemistry publications.

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