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1-Benzyl-3-phenylazetidine

Base Information
  • Chemical Name:1-Benzyl-3-phenylazetidine
  • CAS No.:7215-16-9
  • Molecular Formula:C16H17N
  • Molecular Weight:223.318
  • Hs Code.:2933990090
  • DSSTox Substance ID:DTXSID60222483
  • Nikkaji Number:J84.663E
  • Wikidata:Q83100723
  • Mol file:7215-16-9.mol
1-Benzyl-3-phenylazetidine

Synonyms:1-Benzyl-3-phenylazetidine;7215-16-9;AZETIDINE, 1-BENZYL-3-PHENYL-;L 2237;BRN 1428449;DTXSID60222483;LS-23054;L-2237

Suppliers and Price of 1-Benzyl-3-phenylazetidine
Supply Marketing:
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
  • Chemenu
  • 1-benzyl-3-phenylazetidine 95%
  • 1g
  • $ 439.00
  • Alichem
  • 1-Benzyl-3-phenylazetidine
  • 1g
  • $ 394.16
Total 3 raw suppliers
Chemical Property of 1-Benzyl-3-phenylazetidine
Chemical Property:
  • Vapor Pressure:0.000132mmHg at 25°C 
  • Melting Point:187.5-188.5 °C(Solv: ethyl acetate (141-78-6); methanol (67-56-1)) 
  • Boiling Point:334°Cat760mmHg 
  • PKA:8.22±0.10(Predicted) 
  • Flash Point:141.3°C 
  • PSA:3.24000 
  • Density:1.091g/cm3 
  • LogP:3.22390 
  • Storage Temp.:2-8°C 
  • XLogP3:3.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:3
  • Exact Mass:223.136099547
  • Heavy Atom Count:17
  • Complexity:220
Purity/Quality:

1-benzyl-3-phenylazetidine 95% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1C(CN1CC2=CC=CC=C2)C3=CC=CC=C3
Technology Process of 1-Benzyl-3-phenylazetidine

There total 4 articles about 1-Benzyl-3-phenylazetidine 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 N-ethyl-N,N-diisopropylamine; In acetonitrile; at 70 ℃;
DOI:10.1021/jo061147x
Guidance literature:
allylbenzene; With trifluoromethylsulfonic anhydride; 1,1'-sulfinylbisbenzene; In dichloromethane; at -78 ℃; for 0h; Schlenk technique;
benzylamine; In dichloromethane; at 20 ℃; for 12h; Schlenk technique;
DOI:10.1039/c6cc05128f
Guidance literature:
Multi-step reaction with 2 steps
1: ethyldiisopropylamine / acetonitrile / -20 - -10 °C
2: ethyldiisopropylamine / acetonitrile / 70 °C
With N-ethyl-N,N-diisopropylamine; In acetonitrile;
DOI:10.1021/jo061147x
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