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Pericine

Base Information Edit
  • Chemical Name:Pericine
  • CAS No.:84638-28-8
  • Molecular Formula:C19H22N2
  • Molecular Weight:278.397
  • Hs Code.:
  • UNII:56UJL0958V
  • DSSTox Substance ID:DTXSID101018405
  • Nikkaji Number:J3.302.983G,J2.331.259J
  • Wikipedia:Pericine
  • Wikidata:Q7168395
  • Mol file:84638-28-8.mol
Pericine

Synonyms:pericine

Suppliers and Price of Pericine
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
  • American Custom Chemicals Corporation
  • PERICINE 95.00%
  • 5MG
  • $ 496.42
Total 16 raw suppliers
Chemical Property of Pericine Edit
Chemical Property:
  • Vapor Pressure:2.02E-08mmHg at 25°C 
  • Boiling Point:453.7°C at 760 mmHg 
  • Flash Point:228.2°C 
  • PSA:19.03000 
  • Density:1.15g/cm3 
  • LogP:3.94330 
  • XLogP3:3.2
  • Hydrogen Bond Donor Count:1
  • Hydrogen Bond Acceptor Count:1
  • Rotatable Bond Count:0
  • Exact Mass:278.178298710
  • Heavy Atom Count:21
  • Complexity:453
Purity/Quality:

99% *data from raw suppliers

PERICINE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CC=C1CN2CCC1C(=C)C3=C(CC2)C4=CC=CC=C4N3
  • Isomeric SMILES:C/C=C\1/CN2CC[C@H]1C(=C)C3=C(CC2)C4=CC=CC=C4N3
Technology Process of Pericine

There total 34 articles about Pericine 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:
2-[(E)-2-ethylidene-11b-(hydroxymethyl)-2,3,5,6,11,11b-hexahydro-1H-indolizino(8,7-b)indol-1-yl]ethan-1-ol; With dmap; triethylamine; p-toluenesulfonyl chloride; In tetrahydrofuran; at 0 - 25 ℃; for 6h;
With lithium bromide; In tetrahydrofuran; for 3h; Reflux;
With zinc; In tetrahydrofuran; for 3h; Reflux;
DOI:10.1021/acs.joc.7b02122
Guidance literature:
(+)-2-[(1S,11bS,E)-2-ethylidene-11b-(hydroxymethyl)-2,3,5,6,11,11b-hexahydro-1H-indolizino(8,7-b)indol-1-yl]ethan-1-ol; With dmap; triethylamine; p-toluenesulfonyl chloride; In tetrahydrofuran; at 0 - 25 ℃; for 6h;
With lithium bromide; In tetrahydrofuran; for 3h; Reflux;
With zinc; In tetrahydrofuran; for 3h; Reflux;
DOI:10.1021/acs.joc.7b02122
Guidance literature:
With sodium tetrahydroborate; In methanol;
DOI:10.1016/j.tetlet.2006.05.095
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