Anacyclin

Base Information

Chemical Name:Anacyclin
CAS No.:502-57-8
Molecular Formula:C₁₈H₂₅NO
Molecular Weight:271.403
Hs Code.:
DSSTox Substance ID:DTXSID701184838
Metabolomics Workbench ID:70147
Nikkaji Number:J358.117I
Wikidata:Q27105770

Synonyms:Anacyclin;AC1NQY2W;C08396;(2E,4E)-N-(2-Methylpropyl)-2,4-tetradecadiene-8,10-diynamide;(2E,4E)-N-(2-methylpropyl)tetradeca-2,4-dien-8,10-diynamide;(2E,4E)-N-isobutyltetradeca-2,4-dien-8,10-diynamide;502-57-8;CHEBI:2698;DTXSID701184838;LMFA08020165;94413-18-0;Q27105770

Suppliers and Price of Anacyclin

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

Total 0 raw suppliers

Chemical Property of Anacyclin

Chemical Property:

XLogP3:4.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:8
Exact Mass:271.193614421
Heavy Atom Count:20
Complexity:457

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCC#CC#CCCC=CC=CC(=O)NCC(C)C
Isomeric SMILES:CCCC#CC#CCC/C=C/C=C/C(=O)NCC(C)C

Technology Process of Anacyclin

There total 14 articles about Anacyclin 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: 65.0%

: 14752-60-4
pentynyl bromide

: 18679-26-0
N-isobutyl-nona-2t,4t-dien-8-ynamide

: 502-57-8,94413-18-0
anacycline

Guidance literature:: DOI:10.1016/S0040-4039(00)96649-8

Reference yield:

: 1578-34-3
hexa-1,5-diyn-1-yltrimethylsilane

: 502-57-8,94413-18-0
anacycline

Guidance literature:: Multi-step reaction with 3 steps

1: 1.) Cp₂ZrCl(H) / 2.) (Ph₃P)2Pd(O) / 1.) RT, benzene, 2.) solvent: THF-C₆H₆

2: 90 percent / tetrabutylammonium fluoride / tetrahydrofuran

3: 65 percent

With Schwartz's reagent; tetrabutyl ammonium fluoride; bis(triphenylphosphine)palladium⁽⁰⁾; In tetrahydrofuran;
DOI:10.1016/S0040-4039(00)96649-8

Reference yield:

: 110922-33-3
(E)-N-(2-methylpropyl)-3-bromoacrylamide

: 502-57-8,94413-18-0
anacycline

Guidance literature:: Multi-step reaction with 4 steps

1: NaI, AlCl₃ / acetone

2: 1.) Cp₂ZrCl(H) / 2.) (Ph₃P)2Pd(O) / 1.) RT, benzene, 2.) solvent: THF-C₆H₆

3: 90 percent / tetrabutylammonium fluoride / tetrahydrofuran

4: 65 percent

With Schwartz's reagent; aluminium trichloride; tetrabutyl ammonium fluoride; sodium iodide; bis(triphenylphosphine)palladium⁽⁰⁾; In tetrahydrofuran; acetone;
DOI:10.1016/S0040-4039(00)96649-8