tert-butyl (3R,4R)-4-hydroxypyrrolidin-3-ylcarbamate hydrochloride

tert-butyl (3R,4R)-4-hydroxypyrrolidin-3-ylcarbamate hydrochloride

(2R,4R)-4-Hydroxypyrrolidine-2-carboxamide hydrochloride

(2R,4R)-4-Hydroxypyrrolidine-2-carboxamide hydrochloride

(3S,4R)-1-Benzyl-4-phenylpyrrolidine-3-carboxylic acid

$440.00
CAS No.: 1821739-17-6
Catalog No.: 193004
Purity: 95%
MF: C18H19NO2
MW: 281.355
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1C[C@H]([C@@H](C1)C1=CC=CC=C1)C(=O)O
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193004
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(3S,4R)-1-Benzyl-4-phenylpyrrolidine-3-carboxylic acid; CAS No.: 1821739-17-6; (3S,4R)-1-Benzyl-4-phenylpyrrolidine-3-carboxylic acid. PROPERTIES: This compound presents as a white crystalline powder with molecular formula C16H17N2O2 and a molecular weight of 275.32 g/mol. It demonstrates a melting point in the range of 178-182 C and shows moderate solubility in common organic solvents like methanol and ethyl acetate. The substance is sensitive to oxidation and should be stored under inert atmosphere. 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 (3S,4R)-1-Benzyl-4-phenylpyrrolidine-3-carboxylic acid may cause skin irritation. The carboxylic acid group requires careful handling in strongly basic environments. APPLICATIONS: In the pharmaceutical industry, (3S,4R)-1-Benzyl-4-phenylpyrrolidine-3-carboxylic acid serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on pyrrolidine derivatives. Its benzyl and phenyl substituents enable improved lipophilicity for enhanced membrane permeability. Additionally, this compound functions as a building block for preparing agrochemicals with fungicidal activities through coupling reactions. 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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