(S)-Dodecyloxirane

Base Information Edit

Chemical Name:(S)-Dodecyloxirane
CAS No.:130404-10-3
Molecular Formula:C₁₄H₂₈O
Molecular Weight:212.376
Hs Code.:
European Community (EC) Number:603-414-5
UNII:36PZ0QX26S
DSSTox Substance ID:DTXSID101318976
Nikkaji Number:J971.540A
Wikidata:Q27256587
Mol file:130404-10-3.mol

Synonyms:(S)-Dodecyloxirane;(S)-2-Dodecyloxirane;2-Dodecyl oxirane, (S)-;Oxirane, dodecyl-, (S)-;(-)-1,2-Epoxytetradecane;Oxirane, dodecyl-, (2S)-;Oxirane, 2-dodecyl-, (2S)-;130404-10-3;36PZ0QX26S;UNII-36PZ0QX26S;(S)-2-dodecyl oxirane;(2S)-2-Dodecyloxirane;SCHEMBL12977808;DTXSID101318976;Q27256587

Suppliers and Price of (S)-Dodecyloxirane

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

Total 0 raw suppliers

Chemical Property of (S)-Dodecyloxirane Edit

Chemical Property:

Vapor Pressure:0.00163mmHg at 25°C
XLogP3:6.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:11
Exact Mass:212.214015512
Heavy Atom Count:15
Complexity:133

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCCCCCCCCCCCC1CO1
Isomeric SMILES:CCCCCCCCCCCC[C@H]1CO1

Technology Process of (S)-Dodecyloxirane

There total 11 articles about (S)-Dodecyloxirane 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: 82.0%

: 124-25-4,511542-15-7
myristylaldehyde

: 3234-28-4,130321-67-4,130404-10-3,116619-64-8
(R)-(+)-1,2-epoxytetradecane

Guidance literature:: myristylaldehyde; With (2R,5S)-2-tert-butyl 3,5-dimethylimidazolidin-4-one trifluoroacetic acid salt; 2,2,3,4,5,6-hexachloro-cyclohexa-2,4-dien-1-one; In tetrahydrofuran; at 20 ℃;

With sodium tetrahydroborate; In tetrahydrofuran; ethanol; at 0 - 20 ℃;

With potassium hydroxide; In tetrahydrofuran; ethanol; water; at 20 ℃;
DOI:10.3390/molecules24112081

Reference yield: 43.0%

: 3234-28-4
1,2-epoxytetradecane

: 3234-28-4,130321-67-4,130404-10-3,116619-64-8
(R)-(+)-1,2-epoxytetradecane

: 153062-87-4
(S)-tetradecane-1,2-diol

Guidance literature:: With water; (R,R)-Co(III)(salen)*OAc; at 0 ℃; for 24h;
DOI:10.1055/s-2007-991056

Reference yield: 42.0%

: 3234-28-4
1,2-epoxytetradecane

: 153062-86-3
(R)-tetradecane-1,2-diol

: 3234-28-4,130321-67-4,130404-10-3,116619-64-8
(R)-(+)-1,2-epoxytetradecane

: 153062-87-4
(S)-tetradecane-1,2-diol

Guidance literature:: With [(R,R)-N,N'-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexanediaminato^(2-)]cobalt(III) acetate; water; In isopropyl alcohol; at 20 ℃; for 24h;
DOI:10.1021/ja016737l