4-Cyclopentadecyn-1-one

Base Information

Chemical Name:4-Cyclopentadecyn-1-one
CAS No.:14224-80-7
Molecular Formula:C15H24O
Molecular Weight:220.355
Hs Code.:
European Community (EC) Number:604-281-6
DSSTox Substance ID:DTXSID501318885
Nikkaji Number:J811.047F

Synonyms:4-Cyclopentadecyn-1-one;SCHEMBL10877509;DTXSID501318885;14224-80-7

Suppliers and Price of 4-Cyclopentadecyn-1-one

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 2 raw suppliers

Chemical Property of 4-Cyclopentadecyn-1-one

Chemical Property:

Vapor Pressure:5.37E-05mmHg at 25°C
XLogP3:4.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:220.182715385
Heavy Atom Count:16
Complexity:253

Purity/Quality:: 99.9% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCCCCC(=O)CCC#CCCCC1

Technology Process of 4-Cyclopentadecyn-1-one

There total 9 articles about 4-Cyclopentadecyn-1-one 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: 70.0%

: bicyclo[10.3.0]pentadec-[1⁽¹²⁾]en-13-one p-toluenesulphonyl-hydrazone

: 14224-80-7
cyclopentadec-4-yn-1-one

Guidance literature:: With 1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; In isopropyl alcohol; at -20 ℃; for 0.05h; Temperature; Solvent; Inert atmosphere;

Reference yield:

: 15210-25-0
bicyclo[10.3.0]pentadec-1⁽¹²⁾-en-13-one

: 14224-80-7
cyclopentadec-4-yn-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: 61 percent / aq. ethanol / 7 h / Heating

2: 1.) Bu₄NClO₄, MeOH, 2.) 0.1 N aq. H₂SO₄ / 1.) MeCN, RT, anodic oxidation: graphite anode, stainless steel cathode; 0.05 A/cm², 4.7 V, 4 F/mol

With methanol; sulfuric acid; tetrabutylammonium perchlorate; In ethanol;
DOI:10.1002/hlca.19890720627