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Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)-

Base Information Edit
  • Chemical Name:Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)-
  • CAS No.:150988-85-5
  • Molecular Formula:C26H43NO4
  • Molecular Weight:433.632
  • Hs Code.:
  • DSSTox Substance ID:DTXSID80164679
  • Nikkaji Number:J572.104K
  • Wikidata:Q76278903
  • Mol file:150988-85-5.mol
Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)-

Synonyms:Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)-;N-((4-Hydroxy-3-methoxyphenyl)methyl)-3-octyloxiraneoctanamide cis-(+-)-;150988-85-5;C26-H43-N-O4;DTXSID80164679;LS-101092;(9R,10S)-N-(4-Hydroxy-3-methoxybenzyl)-9,10-epoxyoctadecanamide

Suppliers and Price of Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
Manufacturers and distributors:
  • Manufacture/Brand
  • Chemicals and raw materials
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Chemical Property of Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)- Edit
Chemical Property:
  • Vapor Pressure:1.91E-15mmHg at 25°C 
  • Boiling Point:609.4°Cat760mmHg 
  • Flash Point:322.4°C 
  • Density:1.024g/cm3 
  • XLogP3:7
  • Hydrogen Bond Donor Count:2
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:18
  • Exact Mass:433.31920885
  • Heavy Atom Count:31
  • Complexity:472
Purity/Quality:
Safty Information:
  • Pictogram(s):  
  • Hazard Codes: 
MSDS Files:

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCC1C(O1)CCCCCCCC(=O)NCC2=CC(=C(C=C2)O)OC
  • Isomeric SMILES:CCCCCCCC[C@H]1[C@H](O1)CCCCCCCC(=O)NCC2=CC(=C(C=C2)O)OC
Technology Process of Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)-

There total 6 articles about Oxiraneoctanamide, N-((4-hydroxy-3-methoxyphenyl)methyl)-3-octyl-, cis-(+-)- 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 3-chloro-benzenecarboperoxoic acid;
DOI:10.1021/jm00070a002
Guidance literature:
Multi-step reaction with 2 steps
1: 85 percent / dimethylformamide; diethyl ether / Ambient temperature
2: 53 percent / m-chloroperbenzoic acid (m-CPBA)
With 3-chloro-benzenecarboperoxoic acid; In diethyl ether; N,N-dimethyl-formamide;
DOI:10.1021/jm00070a002
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