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(E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN

Base Information
  • Chemical Name:(E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN
  • CAS No.:311351-26-5
  • Molecular Formula:C18H22 I N O2
  • Molecular Weight:411.28
  • Hs Code.:
  • Mol file:311351-26-5.mol
(E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN

Synonyms:8-Azabicyclo[3.2.1]octane-2-carboxylicacid, 8-[(2E)-3-iodo-2-propenyl]-3-(4-methylphenyl)-, (1R,2S,3S,5S)- (9CI);Nor-PE 2I

Suppliers and Price of (E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN
Supply Marketing:
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
  • TRC
  • Nor-PE2I
  • 1mg
  • $ 220.00
  • TRC
  • Nor-PE2I
  • 10mg
  • $ 1650.00
  • TRC
  • Nor-PE2I
  • 5mg
  • $ 935.00
  • American Custom Chemicals Corporation
  • (E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(PARA-TOLYL)NORTROPAN 95.00%
  • 5MG
  • $ 502.58
Total 2 raw suppliers
Chemical Property of (E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN
Chemical Property:
  • Boiling Point:501.7±50.0 °C(Predicted) 
  • PKA:3.68±0.40(Predicted) 
  • PSA:40.54000 
  • Density:1.505±0.06 g/cm3(Predicted) 
  • LogP:3.90270 
  • Storage Temp.:-20°C Freezer 
  • Solubility.:Dichloromethane; Alcohol 
Purity/Quality:

Nor-PE2I *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Uses Nor-PE 2I is an intermediate in the synthesis of Fluoroethyl-PE2I (F591758), which is a useful intermediate that is often used in the synthesis of PET ligands that are used for dopamine transporter imaging.
Technology Process of (E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN

There total 1 articles about (E)-N-3-(IODOPROP-2-ENYL)2E-CARBOXY-3E-(P-TOLYL)-NORTROPAN 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:

Reference yield:

Guidance literature:
In 1,4-dioxane; water; Reflux;
DOI:10.1002/jlcr.2927
Guidance literature:
C18H22INO2; With tetra(n-butyl)ammonium hydroxide; In water; toluene; at 20 ℃; for 0.166667h;
1,2-bis-tosyloxyethane; In acetonitrile; at 20 ℃; for 2h;
DOI:10.1002/jlcr.2927
Guidance literature:
C18H22INO2; With tetra(n-butyl)ammonium hydroxide; In water; toluene; at 20 ℃; for 0.166667h;
2-fluoroethyl tosylate; In N,N-dimethyl-formamide; at 70 ℃; for 1h;
DOI:10.1002/jlcr.2927
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