(2S)-2-[(2-allylphenoxy)methyl]oxirane

Base Information

Chemical Name:(2S)-2-[(2-allylphenoxy)methyl]oxirane
CAS No.:81840-59-7
Molecular Formula:C12H14O2
Molecular Weight:190.242
Hs Code.:
DSSTox Substance ID:DTXSID70359532
Nikkaji Number:J475.259G
Wikidata:Q82140781

Synonyms:(2S)-2-[(2-allylphenoxy)methyl]oxirane;81840-59-7;SCHEMBL7092232;DTXSID70359532;[S,(+)]-2alpha-[[2-(2-Propenyl)phenoxy]methyl]oxirane

Suppliers and Price of (2S)-2-[(2-allylphenoxy)methyl]oxirane

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 (2S)-2-[(2-allylphenoxy)methyl]oxirane

Chemical Property:

XLogP3:3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:190.099379685
Heavy Atom Count:14
Complexity:191

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CCC1=CC=CC=C1OCC2CO2
Isomeric SMILES:C=CCC1=CC=CC=C1OC[C@@H]2CO2

Technology Process of (2S)-2-[(2-allylphenoxy)methyl]oxirane

There total 11 articles about (2S)-2-[(2-allylphenoxy)methyl]oxirane 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: 100.0%

: 1314092-54-0
(2S)-glycidyl-3-nitrobenzenesulfonate

: 1745-81-9
o-Allylphenol

: 81840-59-7
(S)1-(2’-allylphenoxy)-2,3-epoxypropane

Guidance literature:: o-Allylphenol; With sodium hydride; In N,N-dimethyl-formamide; mineral oil; at 20 ℃; for 0.5h; Inert atmosphere;

(2S)-glycidyl-3-nitrobenzenesulfonate; In N,N-dimethyl-formamide; mineral oil; at 60 ℃;
DOI:10.1021/jm2008562

Reference yield: 65.0%

: 115314-14-2
(2s)-(+)-glycidyl 3-nitrobenzenesulfonate

: 1745-81-9
o-Allylphenol

: 81840-59-7
(S)1-(2’-allylphenoxy)-2,3-epoxypropane

Guidance literature:: o-Allylphenol; With potassium carbonate; In acetone; Inert atmosphere; Reflux;

(2s)-(+)-glycidyl 3-nitrobenzenesulfonate; In acetone; for 21h; Inert atmosphere; Reflux;
DOI:10.1021/acs.jmedchem.9b00595

Reference yield: 43.4%

: 4638-04-4
1-(2-allylphenoxy)-2,3-epoxypropane

: 81840-59-7
(S)1-(2’-allylphenoxy)-2,3-epoxypropane

: (R)-3-(2'-allylphenoxy)-propane-1,2-diol

Guidance literature:: With Bacillus megaterium epoxide hydrolase; In aq. phosphate buffer; di-isopropyl ether; at 25 ℃; pH=7; Enzymatic reaction;
DOI:10.1002/anie.201402653