2-Decyl-1,3-dioxolane

Base Information

Chemical Name:2-Decyl-1,3-dioxolane
CAS No.:6316-24-1
Molecular Formula:C13H26 O2
Molecular Weight:214.348
Hs Code.:
European Community (EC) Number:228-650-2
NSC Number:22579
UNII:65ZW55JA5E
DSSTox Substance ID:DTXSID20212502
Nikkaji Number:J206.906G
Wikidata:Q83087645
Mol file:6316-24-1.mol

Synonyms:2-Decyl-1,3-dioxolane;6316-24-1;1,3-Dioxolane, 2-decyl-;AI3-30691;EINECS 228-650-2;NSC-22579;NSC22579;2-decyl-[1,3]dioxolane;SCHEMBL413367;undecan-11-one ethylene ketal;65ZW55JA5E;DTXSID20212502;NSC 22579

Suppliers and Price of 2-Decyl-1,3-dioxolane

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 7 raw suppliers

Chemical Property of 2-Decyl-1,3-dioxolane

Chemical Property:

Vapor Pressure:0.0164mmHg at 25°C
Boiling Point:263.8°C at 760 mmHg
Flash Point:104.1°C
PSA：18.46000
Density:0.891g/cm³
LogP:3.89010
XLogP3:4.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:9
Exact Mass:214.193280068
Heavy Atom Count:15
Complexity:131

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCCCCCC1OCCO1

Technology Process of 2-Decyl-1,3-dioxolane

There total 6 articles about 2-Decyl-1,3-dioxolane 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: 99.0%

: 112-44-7
undecylaldehyde

: 107-21-1
ethylene glycol

: 6316-24-1
undecanal ethylene acetal

Guidance literature:: With diphenylamine-terephthalaldehyde resin p-toluenesulfonate with high sulfo group content; In toluene; for 0.333333h; Reagent/catalyst; chemoselective reaction; Dean-Stark; Reflux;
DOI:10.1246/cl.150166

Reference yield: 24.0%

: 872-05-9,17438-89-0,25189-70-2
1-Decene

: 201230-82-2
carbon monoxide

: 107-21-1
ethylene glycol

: 6316-24-1
undecanal ethylene acetal

Guidance literature:: With mer-[RuCl₃(1,4-bis(diphenylphosphino)butane)(4-phenylpyridine)]; hydrogen; at 160 ℃; for 24h; under 67506.8 Torr; Catalytic behavior;
DOI:10.1016/j.molcata.2016.09.020