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1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone

Base Information Edit
  • Chemical Name:1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone
  • CAS No.:148260-92-8
  • Molecular Formula:C26H27 N O3
  • Molecular Weight:401.505
  • Hs Code.:
  • UNII:T0H910M40A
  • DSSTox Substance ID:DTXSID50933354
  • Nikkaji Number:J591.785I
  • Wikipedia:SCH-48461
  • Wikidata:Q7389138
  • ChEMBL ID:CHEMBL23541
  • Mol file:148260-92-8.mol
1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone

Synonyms:1,4-bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone;SCH 48461;SCH-48461

Suppliers and Price of 1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
  • Packaging
  • price
Total 1 raw suppliers
Chemical Property of 1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone Edit
Chemical Property:
  • Vapor Pressure:2.32E-15mmHg at 25°C 
  • Boiling Point:621.3°Cat760mmHg 
  • Flash Point:329.6°C 
  • PSA:38.77000 
  • Density:1.148g/cm3 
  • LogP:5.49580 
  • XLogP3:5.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:3
  • Rotatable Bond Count:8
  • Exact Mass:401.19909372
  • Heavy Atom Count:30
  • Complexity:530
Purity/Quality:

99%min *data from raw suppliers

Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C2C(C(=O)N2C3=CC=C(C=C3)OC)CCCC4=CC=CC=C4
  • Isomeric SMILES:COC1=CC=C(C=C1)[C@@H]2[C@H](C(=O)N2C3=CC=C(C=C3)OC)CCCC4=CC=CC=C4
Technology Process of 1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone

There total 18 articles about 1,4-Bis(4-methoxyphenyl)-3-(3-phenylpropyl)-2-azetidinone 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:
Guidance literature:
With potassium tert-butylate; In tetrahydrofuran; at 0 ℃; Yield given;
DOI:10.1016/0040-4039(94)85308-8
Guidance literature:
Multi-step reaction with 2 steps
1: LDA / tetrahydrofuran / -78 °C
2: 20percent KOBu-t / tetrahydrofuran / 0 °C
With potassium tert-butylate; lithium diisopropyl amide; In tetrahydrofuran;
DOI:10.1016/0040-4039(94)85308-8
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / pyridine / CH2Cl2 / 2 h / Ambient temperature
2: 1.) LDA / 1.) THF, hexane, from -78 to -65 deg C, 2 h, 2.) THF, hexane, from -78 deg C to RT, 15 h
With pyridine; lithium diisopropyl amide; In dichloromethane;
DOI:10.1055/s-1996-4302
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