Ethanone, 1-(1-cycloocten-1-yl)-

Base Information

Chemical Name:Ethanone, 1-(1-cycloocten-1-yl)-
CAS No.:17339-74-1
Molecular Formula:C10H16O
Molecular Weight:
Hs Code.:
European Community (EC) Number:466-270-0
Nikkaji Number:J1.652.514F
Wikidata:Q76422881

Synonyms:Ethanone, 1-(1-cycloocten-1-yl)-;1-[(1E)-cycloocten-1-yl]ethanone;Ethanone, 1-(1-cycloocten-1-yl)-, (Z)- (9CI);127649-04-1;17339-74-1;SCHEMBL621702;SCHEMBL1229915;147384-72-3;Ethanone,1-(1-cycloocten-1-yl)-,[s-(Z)]-(9ci)

Suppliers and Price of Ethanone, 1-(1-cycloocten-1-yl)-

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 1 raw suppliers

Chemical Property of Ethanone, 1-(1-cycloocten-1-yl)-

Chemical Property:

Vapor Pressure:0.0301mmHg at 25°C
XLogP3:2.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:152.120115130
Heavy Atom Count:11
Complexity:168

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=O)C1=CCCCCCC1
Isomeric SMILES:CC(=O)/C/1=C/CCCCCC1

Technology Process of Ethanone, 1-(1-cycloocten-1-yl)-

There total 6 articles about Ethanone, 1-(1-cycloocten-1-yl)- 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:

: 931-88-4,931-87-3,25267-51-0
cis-Cyclooctene

: 75-36-5
acetyl chloride

: 17339-74-1,147384-72-3,147384-73-4
1-(cyclooct-1-en-1-yl)ethanone

Guidance literature:: With carbon disulfide; tin(IV) chloride;
DOI:10.1002/hlca.19310140615

Reference yield:

: 502-49-8
cycloactanone

: 1066-54-2
trimethylsilylacetylene

: 17339-74-1,147384-72-3,147384-73-4
1-(cyclooct-1-en-1-yl)ethanone

Guidance literature:: trimethylsilylacetylene; With n-butyllithium; In tetrahydrofuran; at 0 ℃; for 1h; Inert atmosphere;

cycloactanone; In tetrahydrofuran; at 0 - 25 ℃; for 2h; Inert atmosphere;

With sulfuric acid; In methanol; for 12h; Inert atmosphere; Reflux;
DOI:10.1021/acs.orglett.0c02466

Reference yield:

: 502-49-8
cycloactanone

: 17339-74-1,147384-72-3,147384-73-4
1-(cyclooct-1-en-1-yl)ethanone

Guidance literature:: Multi-step reaction with 3 steps

1: diethyl ether; sodium; sodium bicarbonate

2: naphthalene-sulfonic acid-⁽²⁾ / 190 °C

3: SnCl₄; carbon disulfide

With carbon disulfide; diethyl ether; naphthalene-2-sulfonate; sodium; tin(IV) chloride; sodium hydrogencarbonate;
DOI:10.1002/hlca.19310140615