3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)-

Base Information

Chemical Name:3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)-
CAS No.:859-20-1
Molecular Formula:C22H39NO4
Molecular Weight:381.5494
Hs Code.:
DSSTox Substance ID:DTXSID70235226
Wikidata:Q83117106

Synonyms:3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)-;859-20-1;BRN 2298946;12-Ethyl-1-(thymyloxy)-3,6,9-trioxa-12-azatetradecane;DTXSID70235226

Suppliers and Price of 3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)-

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)-

Chemical Property:

Vapor Pressure:1.04E-08mmHg at 25°C
Boiling Point:461.8°Cat760mmHg
Flash Point:119.5°C
Density:0.984g/cm³
XLogP3:4.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:16
Exact Mass:381.28790873
Heavy Atom Count:27
Complexity:336

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCN(CC)CCOCCOCCOCCOC1=C(C=CC(=C1)C)C(C)C

Technology Process of 3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)-

There total 3 articles about 3,6,9-Trioxa-12-azatetradecane, 12-ethyl-1-(thymyloxy)- 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:

: 89-83-8
thymol

: 859-20-1
1-Diethylamino-11-<6-isopropyl-3-methyl-phenoxy>-3,6,9-trioxa-undecan

Guidance literature:: Multi-step reaction with 2 steps

1: (i) NaOH, HOCH₂CH₂OH, (ii) /BRN= 605317/

2: (i) Na, xylene, (ii) /BRN= 2267168/

DOI:10.1021/jm00328a035