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Encyclopedia

9-Tricosyne

Base Information Edit
  • Chemical Name:9-Tricosyne
  • CAS No.:39487-08-6
  • Molecular Formula:C23H44
  • Molecular Weight:320.602
  • Hs Code.:2901299090
  • DSSTox Substance ID:DTXSID3068178
  • Nikkaji Number:J422.402G
  • Wikidata:Q81994890
  • Mol file:39487-08-6.mol
9-Tricosyne

Synonyms:9-Tricosyne;tricos-9-yne;39487-08-6;AI3-35826;DTXSID3068178;C23H44;C23-H44

Suppliers and Price of 9-Tricosyne
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
  • 9-TRICOSYNE 95.00%
  • 5MG
  • $ 504.27
Total 0 raw suppliers
Chemical Property of 9-Tricosyne Edit
Chemical Property:
  • Vapor Pressure:4.75E-06mmHg at 25°C 
  • Boiling Point:393.7°Cat760mmHg 
  • Flash Point:193°C 
  • PSA:0.00000 
  • Density:0.818g/cm3 
  • LogP:8.44150 
  • XLogP3:11.5
  • Hydrogen Bond Donor Count:0
  • Hydrogen Bond Acceptor Count:0
  • Rotatable Bond Count:17
  • Exact Mass:320.344301404
  • Heavy Atom Count:23
  • Complexity:264
Purity/Quality:

9-TRICOSYNE 95.00% *data from reagent suppliers

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

SDS file from LookChem

Useful:
  • Canonical SMILES:CCCCCCCCCCCCCC#CCCCCCCCC
Technology Process of 9-Tricosyne

There total 8 articles about 9-Tricosyne 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 [2,2]bipyridinyl; copper(l) iodide; In tetrahydrofuran; 1) 2 deg C, 2 h, 2) room temperature, 12 h;
DOI:10.1007/BF00574217
Guidance literature:
Multi-step reaction with 2 steps
1: 82 percent / Br2, triphenylphosphine, (C2H5)3N / CCl4 / 12 h / 20 °C
2: 74 percent / CuI, bi-2-pyridyl / tetrahydrofuran / 1) 2 deg C, 2 h, 2) room temperature, 12 h
With [2,2]bipyridinyl; copper(l) iodide; bromine; triethylamine; triphenylphosphine; In tetrahydrofuran; tetrachloromethane;
DOI:10.1007/BF00574217
Guidance literature:
Multi-step reaction with 3 steps
1: 64 percent / Fe acetylacetonate / bis-(2-methoxy-ethyl) ether; diethyl ether; liquid ammonia / from -30 to 30 deg C, 5 h, 30 deg C, 15 h
2: 82 percent / Br2, triphenylphosphine, (C2H5)3N / CCl4 / 12 h / 20 °C
3: 74 percent / CuI, bi-2-pyridyl / tetrahydrofuran / 1) 2 deg C, 2 h, 2) room temperature, 12 h
With [2,2]bipyridinyl; copper(l) iodide; iron(III)-acetylacetonate; bromine; triethylamine; triphenylphosphine; In tetrahydrofuran; tetrachloromethane; diethyl ether; diethylene glycol dimethyl ether; ammonia;
DOI:10.1007/BF00574217
upstream raw materials:

n-chlorooctane

pentadec-1-yne

1-decyne

1-tridecene

Downstream raw materials:

(Z)-tricos-9-ene

trans-9-tricosene

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