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1-(1-(4-Methoxyphenyl)cyclohexyl)piperidine

Base Information Edit
  • Chemical Name:1-(1-(4-Methoxyphenyl)cyclohexyl)piperidine
  • CAS No.:2201-35-6
  • Molecular Formula:C18H27NO
  • Molecular Weight:273.21
  • Hs Code.:2933399090
  • UNII:OZM0C31BLL
  • ChEMBL ID:CHEMBL1760302
  • DSSTox Substance ID:DTXSID40176450
  • Nikkaji Number:J390.368K
  • Wikidata:Q2159639
  • Wikipedia:4-MeO-PCP
  • Mol file:2201-35-6.mol
1-(1-(4-Methoxyphenyl)cyclohexyl)piperidine

Synonyms:1-(1-(4-methoxyphenyl)cyclohexyl)piperidine;4-MeO-phencyclidine

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Chemical Property of 1-(1-(4-Methoxyphenyl)cyclohexyl)piperidine Edit
Chemical Property:
  • Boiling Point:375.086 °C at 760 mmHg 
  • Flash Point:110.59 °C 
  • PSA:12.47000 
  • Density:1.035 g/cm3 
  • LogP:4.27840 
  • XLogP3:3.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:3
  • Exact Mass:273.209264485
  • Heavy Atom Count:20
  • Complexity:284
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C2(CCCCC2)N3CCCCC3
  • Uses Methoxydine contains pharamcological activity and found to be one of novel analogs of ketamine and phencyclidine as NMDA receptor antagonists.
Technology Process of 1-(1-(4-Methoxyphenyl)cyclohexyl)piperidine

There total 5 articles about 1-(1-(4-Methoxyphenyl)cyclohexyl)piperidine 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:
Multi-step reaction with 2 steps
1: toluene / 12 h / 130 °C
2: tetrahydrofuran / -78 - 20 °C
In tetrahydrofuran; toluene;
DOI:10.1016/j.bmcl.2011.02.009
Guidance literature:
Multi-step reaction with 2 steps
1: toluene / 12 h / 130 °C
2: tetrahydrofuran / -78 - 20 °C
In tetrahydrofuran; toluene;
DOI:10.1016/j.bmcl.2011.02.009