trans-(1-Benzylpyrrolidine-3,4-diyl)dimethanol
$250.00
CAS No.: 1345831-65-3
Catalog No.: 192992
Purity: 95%
MF: C13H19NO2
MW: 221.3
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1C[C@H]([C@@H](C1)CO)CO
Catalog No.: 192992
Purity: 95%
MF: C13H19NO2
MW: 221.3
Storage: 2-8 degree Celsius
SMILES: C(C1=CC=CC=C1)N1C[C@H]([C@@H](C1)CO)CO
trans-(1-Benzylpyrrolidine-3,4-diyl)dimethanol; CAS No.: 1345831-65-3; trans-(1-Benzylpyrrolidine-3,4-diyl)dimethanol. PROPERTIES: This compound appears as a white crystalline solid with molecular formula C12H18N2O2 and a molecular weight of 222.28 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 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 trans-(1-Benzylpyrrolidine-3,4-diyl)dimethanol may cause skin irritation. The hydroxyl groups require careful handling in strongly acidic environments. APPLICATIONS: In the pharmaceutical industry, trans-(1-Benzylpyrrolidine-3,4-diyl)dimethanol serves as an intermediate for synthesizing non-steroidal anti-inflammatory drugs (NSAIDs), as described in medicinal chemistry literature focusing on pyrrolidine derivatives. Its hydroxyl substituents enable formation of bioactive esters through esterification reactions. 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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