[(3,4,5-Trimethoxyphenoxy)methyl]oxirane

Base Information

Chemical Name:[(3,4,5-Trimethoxyphenoxy)methyl]oxirane
CAS No.:74760-14-8
Molecular Formula:C12H16 O5
Molecular Weight:240.256
Hs Code.:2910900090
European Community (EC) Number:277-990-8
DSSTox Substance ID:DTXSID50996282
Nikkaji Number:J349.459D
Mol file:74760-14-8.mol

Synonyms:74760-14-8;2-[(3,4,5-trimethoxyphenoxy)methyl]oxirane;[(3,4,5-Trimethoxyphenoxy)methyl]oxirane;EINECS 277-990-8;((3,4,5-Trimethoxyphenoxy)methyl)oxirane;SCHEMBL3266050;DTXSID50996282;DMPSZPVEKHHIBR-UHFFFAOYSA-N;2-(3,4,5-TRIMETHOXYPHENOXYMETHYL)OXIRANE;(+/-)-2-(3,4,5-Trimethoxy-phenoxymethyl)-oxirane

Suppliers and Price of [(3,4,5-Trimethoxyphenoxy)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 3 raw suppliers

Chemical Property of [(3,4,5-Trimethoxyphenoxy)methyl]oxirane

Chemical Property:

Vapor Pressure:8.06E-05mmHg at 25°C
Boiling Point:351.9°C at 760 mmHg
Flash Point:145.9°C
PSA：49.45000
Density:1.167g/cm³
LogP:1.49000
XLogP3:1.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:6
Exact Mass:240.09977361
Heavy Atom Count:17
Complexity:221

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=CC(=C1OC)OC)OCC2CO2

Technology Process of [(3,4,5-Trimethoxyphenoxy)methyl]oxirane

There total 2 articles about [(3,4,5-Trimethoxyphenoxy)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: 90.0%

: 642-71-7
3,4,5-trimethoxyphenol

: 106-89-8,24969-06-0,13403-37-7
epichlorohydrin

: 74760-14-8
1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane

Guidance literature:: With tetrabutylammomium bromide; potassium carbonate; In acetonitrile; at 20 ℃; Reflux;
DOI:10.1055/s-0030-1258173

Reference yield:

: 74760-14-8
1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane

Guidance literature:

Reference yield: 46.0%

: 74760-14-8
1-(3,4,5-trimethoxyphenoxy)-2,3-epoxypropane

: 1254168-43-8
(S)-2-[(3,4,5-trimethoxyphenoxy)methyl]oxirane

: 1254168-46-1
(R)-3-(3,4,5-trimethoxyphenoxy)propane-1,2-diol

Guidance literature:: With (R,R)-Jacobsen catalyst; water; at 0 - 20 ℃; optical yield given as %ee; enantioselective reaction; Resolution of racemate;
DOI:10.1055/s-0030-1258173