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Technology Process of beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone

beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone

Base Information
  • Chemical Name:beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone
  • CAS No.:23902-89-8
  • Molecular Formula:C27H29 Cl N2 O
  • Molecular Weight:433.03
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80946699
  • Nikkaji Number:J41.535I
  • Mol file:23902-89-8.mol
beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone

Synonyms:23902-89-8;beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone;3-(4-chlorophenyl)-3-phenyl-1-[4-(2-phenylethyl)piperazin-1-yl]propan-1-one;1-(3-(p-Chlorophenyl)-3-phenylpropionyl)-4-phenethylpiperazine;KETONE, beta-(p-CHLOROPHENYL)PHENETHYL 4-PHENETHYLPIPERAZINYL;Piperazine, 1-(3-(p-chlorophenyl)-3-phenylpropionyl)-4-phenethyl-;C27H29ClN2O;DTXSID80946699;LS-87110;Piperazine, 1-(p-chloro-.beta.-phenylhydrocinnamoyl)-4-phenethyl-;3-(p-Chlorophenyl)-3-phenyl-1-(4-phenethyl-1-piperazinyl)-1-propanone

Suppliers and Price of beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone
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
Total 5 raw suppliers
Chemical Property of beta-(p-Chlorophenyl)phenethyl 4-phenethylpiperazinyl ketone
Chemical Property:
  • Vapor Pressure:2.8E-14mmHg at 25°C 
  • Refractive Index:1.5790 (estimate) 
  • Boiling Point:598.4°Cat760mmHg 
  • PKA:7.14±0.10(Predicted) 
  • Flash Point:315.7°C 
  • PSA：23.55000 
  • Density:1.166g/cm3 
  • LogP:5.12470 
  • XLogP3:5.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:7
  • Exact Mass:432.1968412
  • Heavy Atom Count:31
  • Complexity:527
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CN(CCN1CCC2=CC=CC=C2)C(=O)CC(C3=CC=CC=C3)C4=CC=C(C=C4)Cl
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