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Technology Process of Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-

Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-

Base Information
  • Chemical Name:Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-
  • CAS No.:13073-72-8
  • Molecular Formula:C25H23 Cl O2
  • Molecular Weight:390.9019
  • Hs Code.:
  • UNII:4U7Y1WZP9X
  • DSSTox Substance ID:DTXSID00926877
  • Wikidata:Q27260514
Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-

Synonyms:BRN 1328056;4U7Y1WZP9X;Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-;13073-72-8;2-(p-Chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-1,2,3,4-tetrahydro naphthalene;2-(p-Chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-1,2,3,4-tetrahydronaphthalene;UNII-4U7Y1WZP9X;C25H23ClO2;C25-H23-Cl-O2;DTXSID00926877;LS-94959;Q27260514;2-({4-[2-(4-chlorophenyl)-1,2,3,4-tetrahydronaphthalen-1-yl]phenoxy}methyl)oxirane;NAPHTHALENE, 2-(P-CHLOROPHENYL)-1-(P-(2,3-EPOXYPROPOXY)PHENYL)-1,2,3,4-TETRAHYDRO-;OXIRANE, 2-((4-(2-(4-CHLOROPHENYL)-1,2,3,4-TETRAHYDRO-1-NAPHTHALENYL)PHENOXY)METHYL)-

Suppliers and Price of Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of Naphthalene, 1,2,3,4-tetrahydro-2-(p-chlorophenyl)-1-(p-(2,3-epoxypropoxy)phenyl)-
Chemical Property:
  • Vapor Pressure:5.79E-10mmHg at 25°C 
  • Boiling Point:508.7°Cat760mmHg 
  • Flash Point:162.7°C 
  • Density:1.218g/cm3 
  • XLogP3:6.3
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:5
  • Exact Mass:390.1386577
  • Heavy Atom Count:28
  • Complexity:495
Purity/Quality:

85.0-99.8% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:C1CC2=CC=CC=C2C(C1C3=CC=C(C=C3)Cl)C4=CC=C(C=C4)OCC5CO5
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