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Pipermethystine

Base Information Edit
  • Chemical Name:Pipermethystine
  • CAS No.:71627-22-0
  • Molecular Formula:C16H17 N O4
  • Molecular Weight:287.315
  • Hs Code.:
  • UNII:APX8C8S6AW
  • DSSTox Substance ID:DTXSID60992199
  • Nikkaji Number:J1.902.829A
  • Wikipedia:Pipermethystine
  • Wikidata:Q7197360
  • Metabolomics Workbench ID:46071
  • Mol file:71627-22-0.mol
Pipermethystine

Synonyms:pipermethystine

Suppliers and Price of Pipermethystine
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
  • Packaging
  • price
Total 34 raw suppliers
Chemical Property of Pipermethystine Edit
Chemical Property:
  • Vapor Pressure:1.22E-08mmHg at 25°C 
  • Boiling Point:459.9°C at 760 mmHg 
  • PKA:-3.19±0.40(Predicted) 
  • Flash Point:231.9°C 
  • PSA:63.68000 
  • Density:1.23g/cm3 
  • LogP:1.41380 
  • XLogP3:1.4
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:4
  • Rotatable Bond Count:5
  • Exact Mass:287.11575802
  • Heavy Atom Count:21
  • Complexity:438
Purity/Quality:

99% *data from raw suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC(=O)OC1CN(C(=O)C=C1)C(=O)CCC2=CC=CC=C2
Technology Process of Pipermethystine

There total 5 articles about Pipermethystine 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 trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 0.0833333h;
DOI:10.1021/ol010183+
Guidance literature:
Multi-step reaction with 5 steps
1.1: 80 percent / RuCl2(PCy3)2CHPh / CH2Cl2 / 12 h / Heating
2.1: n-BuLi / tetrahydrofuran; hexane / 0.25 h / -78 °C
2.2: 94 percent / tetrahydrofuran; hexane / 0.17 h / -78 °C
3.1: 91 percent / MCPBA / CH2Cl2 / 15 h / 20 °C
4.1: 99 percent / t-BuOK / 2-methyl-propan-2-ol / 20 °C
5.1: 98 percent / TMSOTf / CH2Cl2 / 0.08 h / 0 °C
With Grubbs catalyst first generation; n-butyllithium; trimethylsilyl trifluoromethanesulfonate; potassium tert-butylate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; hexane; dichloromethane; tert-butyl alcohol;
DOI:10.1021/ol010183+
Guidance literature:
Multi-step reaction with 4 steps
1.1: n-BuLi / tetrahydrofuran; hexane / 0.25 h / -78 °C
1.2: 94 percent / tetrahydrofuran; hexane / 0.17 h / -78 °C
2.1: 91 percent / MCPBA / CH2Cl2 / 15 h / 20 °C
3.1: 99 percent / t-BuOK / 2-methyl-propan-2-ol / 20 °C
4.1: 98 percent / TMSOTf / CH2Cl2 / 0.08 h / 0 °C
With n-butyllithium; trimethylsilyl trifluoromethanesulfonate; potassium tert-butylate; 3-chloro-benzenecarboperoxoic acid; In tetrahydrofuran; hexane; dichloromethane; tert-butyl alcohol;
DOI:10.1021/ol010183+
Refernces Edit
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