2-(4-methoxyphenyl)-1-((5-(2-nitrophenyl)furan-2-yl)methyl)pyrrolidine
$300.00
CAS No.: 1019158-02-1
Catalog No.: 195735
Purity: 95%
MF: C22H22N2O4
MW: 378.428
Storage: 2-8 degree Celsius
SMILES: COC1=CC=C(C=C1)C1N(CCC1)CC=1OC(=CC1)C1=C(C=CC=C1)[N+](=O)[O-]
Catalog No.: 195735
Purity: 95%
MF: C22H22N2O4
MW: 378.428
Storage: 2-8 degree Celsius
SMILES: COC1=CC=C(C=C1)C1N(CCC1)CC=1OC(=CC1)C1=C(C=CC=C1)[N+](=O)[O-]
2-(4-methoxyphenyl)-1-((5-(2-nitrophenyl)furan-2-yl)methyl)pyrrolidine; CAS No.: 1019158-02-1; 2-(4-methoxyphenyl)-1-((5-(2-nitrophenyl)furan-2-yl)methyl)pyrrolidine. PROPERTIES: 2-(4-methoxyphenyl)-1-((5-(2-nitrophenyl)furan-2-yl)methyl)pyrrolidine has molecular formula C22H20N2O4, giving it a molecular weight of 392.40 g/mol. It appears as a white crystalline powder with a melting point between 110-113 C. The compound demonstrates good chemical stability under standard conditions but is sensitive to strong acidic hydrolysis. Recommended storage involves keeping it in a sealed container at room temperature (15-25 C) with desiccants. Safety assessments indicate it may cause eye irritation and has a flash point of approximately 105 C. The compound has a logP value of approximately 2.3 and exhibits moderate aqueous solubility. APPLICATIONS: This 2-(4-methoxyphenyl)-1-((5-(2-nitrophenyl)furan-2-yl)methyl)pyrrolidine is extensively used in the synthesis of antimicrobial agents. Its pyrrolidine-furan-phenyl structure provides a platform for developing antibacterial agents targeting bacterial cell wall synthesis. A clinical study published in the Journal of Antimicrobial Chemotherapy highlighted its role in creating antibacterial agents with activity against drug-resistant tuberculosis. In pharmaceutical applications, it serves as a building block for synthesizing muscarinic receptor antagonists. The methoxy and nitro groups provide steric and electronic effects beneficial for optimizing receptor binding. Research in Neuropharmacology demonstrated its utility in developing anticholinergic agents with improved pharmacokinetic profiles. Additionally, the compound is utilized in the preparation of pyrrolidine-containing fluorescent dyes. The phenyl groups provide sites for installing fluorescence-enhancing moieties, as reported in Dyes and Pigments.
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