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Technology Process of 2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate

2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate

Base Information
  • Chemical Name:2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate
  • CAS No.:76823-83-1
  • Molecular Formula:C41H41ClN2O7
  • Molecular Weight:709.22644
  • Hs Code.:
  • European Community (EC) Number:278-558-1
  • Mol file:76823-83-1.mol
2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate

Synonyms:76823-83-1;EINECS 278-558-1;2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate;2-(3-benzoylphenyl)propanoyl 2-[2-[4-[(4-chlorophenyl)benzyl]piperazin-1-yl]ethoxy]ethyl maleate;2-(3-BENZOYLPHENYL)PROPIONOYL 2-[2-[4-[(4-CHLOROPHENYL)BENZYL]PIPERAZIN-1-YL]ETHOXY]ETHYL MALEATE;C37H39ClN2O4.C4H4O4;C37-H39-Cl-N2-O4.C4-H4-O4

Suppliers and Price of 2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 3 raw suppliers
Chemical Property of 2-(3-Benzoylphenyl)propionoyl 2-(2-(4-((4-chlorophenyl)benzyl)piperazin-1-yl)ethoxy)ethyl maleate
Chemical Property:
  • Vapor Pressure:3.96E-26mmHg at 25°C 
  • Boiling Point:807.6°C at 760 mmHg 
  • Flash Point:442.2°C 
  • PSA：102.45000 
  • Density:1.238g/cm3 
  • LogP:6.14330 
  • XLogP3:7
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:9
  • Rotatable Bond Count:18
  • Exact Mass:708.2602293
  • Heavy Atom Count:51
  • Complexity:1140
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(C1=CC(=CC=C1)C(=O)C2=CC=CC=C2)C(=O)OC(=O)C=CC(=O)OCCOCCN3CCN(CC3)C(C4=CC=CC=C4)C5=CC=C(C=C5)Cl
  • Isomeric SMILES:CC(C1=CC(=CC=C1)C(=O)C2=CC=CC=C2)C(=O)OC(=O)/C=C\C(=O)OCCOCCN3CCN(CC3)C(C4=CC=CC=C4)C5=CC=C(C=C5)Cl
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