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

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

benzyl 3,3-difluoropyrrolidine-1-carboxylate

benzyl 3,3-difluoropyrrolidine-1-carboxylate

tert-butyl (3R,5S)-5-methylpyrrolidin-3-ylcarbamate

$375.00
CAS No.: 1626343-40-5
Catalog No.: 192998
Purity: 95%
MF: C10H20N2O2
MW: 200.282
Storage: 2-8 degree Celsius
SMILES: C[C@H]1C[C@H](CN1)NC(OC(C)(C)C)=O
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tert-butyl (3R,5S)-5-methylpyrrolidin-3-ylcarbamate; CAS No.: 1626343-40-5; tert-butyl (3R,5S)-5-methylpyrrolidin-3-ylcarbamate. PROPERTIES: This compound presents as a white crystalline powder with molecular formula C10H18N2O2 and a molecular weight of 194.26 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 tert-butyl (3R,5S)-5-methylpyrrolidin-3-ylcarbamate may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, tert-butyl (3R,5S)-5-methylpyrrolidin-3-ylcarbamate serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on pyrrolidine derivatives. Its methyl substituent enables improved solubility in biological systems for enhanced bioavailability. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through formation of urea derivatives. Academic research has explored its potential in metal coordination chemistry for creating luminescent sensors, as reported in inorganic chemistry journals. The pyrrolidine ring system also facilitates formation of metal-organic frameworks (MOFs), making it valuable for gas storage applications in materials science, as evidenced by studies in crystallography publications.

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