cis-3-(m-Methoxyphenyl)-1-(3-phenylallyl)-3-propylpyrrolidine

Base Information

• Chemical Name: cis-3-(m-Methoxyphenyl)-1-(3-phenylallyl)-3-propylpyrrolidine
• CAS No.: 27019-34-7
• Molecular Formula: C₂₃H₂₉NO
• Molecular Weight: 335.489
• Hs Code.: 2933990090
• Mol file: 27019-34-7.mol

Synonyms:BRN 1495599;cis-3-(m-Methoxyphenyl)-1-(3-phenylallyl)-3-propylpyrrolidine;Pyrrolidine, 3-(m-methoxyphenyl)-1-(3-phenylallyl)-3-propyl-, Z-;27019-34-7;Pyrrolidine, 3-(3-methoxyphenyl)-1-(3-phenyl-2-propenyl)-3-propyl-, (Z)-;LS-138007

Chemical Property of cis-3-(m-Methoxyphenyl)-1-(3-phenylallyl)-3-propylpyrrolidine

Chemical Property:

• Vapor Pressure: 3.56E-09mmHg at 25°C
• Boiling Point: 474.6°Cat760mmHg
• Flash Point: 138°C
• PSA: 12.47000
• Density: 1.026g/cm³
• LogP: 5.09010
• XLogP3: 5.7
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 7
• Exact Mass: 335.224914549
• Heavy Atom Count: 25
• Complexity: 414

Purity/Quality:

99% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCCC1(CCN(C1)CC=CC2=CC=CC=C2)C3=CC(=CC=C3)OC
• Isomeric SMILES: CCCC1(CCN(C1)C/C=C\C2=CC=CC=C2)C3=CC(=CC=C3)OC

Technology Process of cis-3-(m-Methoxyphenyl)-1-(3-phenylallyl)-3-propylpyrrolidine

There total 1 articles about cis-3-(m-Methoxyphenyl)-1-(3-phenylallyl)-3-propylpyrrolidine which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

→ 3-(3-Methoxy-phenyl)-1-((Z)-3-phenyl-allyl)-3-propyl-pyrrolidine (27019-34-7)

Guidance literature:

Acetylen-verb. 47, H2, Pd-CaCO3 (Chinolin vergiftet);

DOI:10.1021/jm00299a002

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