tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate

tert-butyl trans-3,4-diaminopyrrolidine-1-carboxylate

1-(tert-butyl) 2-ethyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate hydrochloride

1-(tert-butyl) 2-ethyl (2S,4R)-4-aminopyrrolidine-1,2-dicarboxylate hydrochloride

tert-butyl ((3S,4R)-4-methylpyrrolidin-3-yl)carbamate hydrochloride

$375.00
CAS No.: 2173637-29-9
Catalog No.: 193013
Purity: 95%
MF: C10H21ClN2O2
MW: 236.743
Storage: 2-8 degree Celsius
SMILES: Cl.C(C)(C)(C)OC(N[C@@H]1CNC[C@H]1C)=O
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193013
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tert-butyl ((3S,4R)-4-methylpyrrolidin-3-yl)carbamate hydrochloride; CAS No.: 2173637-29-9; tert-butyl ((3S,4R)-4-methylpyrrolidin-3-yl)carbamate hydrochloride. PROPERTIES: This compound presents as a white to off-white crystalline solid with molecular formula C10H18N2O2 {HCl and a molecular weight of 220.72 g/mol. It exhibits a melting point in the range of 142-146 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 ((3S,4R)-4-methylpyrrolidin-3-yl)carbamate hydrochloride may cause skin irritation. The carbamate group requires careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, tert-butyl ((3S,4R)-4-methylpyrrolidin-3-yl)carbamate hydrochloride 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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