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2-(4-Methoxyphenyl)cyclohexanone

Base Information
  • Chemical Name:2-(4-Methoxyphenyl)cyclohexanone
  • CAS No.:37087-68-6
  • Molecular Formula:C13H16O2
  • Molecular Weight:204.269
  • Hs Code.:
  • NSC Number:78469
  • DSSTox Substance ID:DTXSID30291823
  • Nikkaji Number:J836.563F
  • Mol file:37087-68-6.mol
2-(4-Methoxyphenyl)cyclohexanone

Synonyms:2-(4-methoxyphenyl)cyclohexanone;37087-68-6;2-(4-methoxyphenyl)cyclohexan-1-one;2-(4-METHOXYPHENYL)-1-CYCLOHEXANONE;NSC78469;SCHEMBL318066;DTXSID30291823;BEBTXYAQBNBPJY-UHFFFAOYSA-N;2-(4-Methoxyphenyl)-cyclohexanone;NSC-78469;AKOS011898125;2-(4-methoxyphenyl)-cyclohexan-1-one;EN300-1153059

Suppliers and Price of 2-(4-Methoxyphenyl)cyclohexanone
Supply Marketing:
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
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Chemical Property of 2-(4-Methoxyphenyl)cyclohexanone
Chemical Property:
  • Vapor Pressure:0.000118mmHg at 25°C 
  • Boiling Point:335.7°Cat760mmHg 
  • Flash Point:149.9°C 
  • PSA:26.30000 
  • Density:1.068g/cm3 
  • LogP:2.92190 
  • XLogP3:2.6
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:2
  • Rotatable Bond Count:2
  • Exact Mass:204.115029749
  • Heavy Atom Count:15
  • Complexity:217
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:COC1=CC=C(C=C1)C2CCCCC2=O
  • Uses 2-(4-Methoxyphenyl)cyclohexanone is a useful synthetic intermediate in the synthesis of rac-14-epi-Dextromethorphan (D299440); an analog of Dextromethorphan (D299445) which is an antitussive compound showing analgesic properties. Dextromethorphan is used in cough medication formulations.
Technology Process of 2-(4-Methoxyphenyl)cyclohexanone

There total 47 articles about 2-(4-Methoxyphenyl)cyclohexanone 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 formic acid; palladium diacetate; 1,2-bis-(diphenylphosphino)ethane; In 1,4-dioxane; at 40 ℃; for 10h; Inert atmosphere; Schlenk technique;
DOI:10.1021/jo5014806
Guidance literature:
With boron trifluoride diethyl etherate; In dichloromethane; at 20 ℃; for 1h; regioselective reaction; Inert atmosphere;
DOI:10.1021/acs.orglett.7b01679
Guidance literature:
With tris-(dibenzylideneacetone)dipalladium(0); Bu3SnF; tri-tert-butyl phosphine; In toluene; for 24h; Inert atmosphere; Reflux;
DOI:10.1021/ja204331w
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