1-Butenyl ethyl ether

Base Information

Chemical Name:1-Butenyl ethyl ether
CAS No.:1528-20-7
Molecular Formula:C6H12O
Molecular Weight:100.161
Hs Code.:
European Community (EC) Number:628-384-0,833-404-8
DSSTox Substance ID:DTXSID501022517
Nikkaji Number:J613.410F

Synonyms:1-BUTENYL ETHYL ETHER;929-05-5;1-ethoxybut-1-ene;1-Ethoxy-1-butene;1528-20-7;cis-1-Butenyl ethyl ether;trans-1-Butenyl ethyl ether;1-Butene, 1-ethoxy-, (E)-;trans-1-Ethoxy-1-butene;SCHEMBL892356;(1E)-1-Butenyl ethyl ether #;AQTYNINXYJFSHD-AATRIKPKSA-N;DTXSID501022517;(1E)-1-ETHOXYBUT-1-ENE;4884-01-9;1-Butenyl ethyl ether, cis + trans;MFCD03427069;AKOS037621867;EN300-137645

Suppliers and Price of 1-Butenyl ethyl ether

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
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price

Total 5 raw suppliers

Chemical Property of 1-Butenyl ethyl ether

Chemical Property:

XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:100.088815002
Heavy Atom Count:7
Complexity:48.1

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

Safty Information:

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MSDS Files:

Useful:

Canonical SMILES:CCC=COCC
Isomeric SMILES:CC/C=C/OCC

Technology Process of 1-Butenyl ethyl ether

There total 1 articles about 1-Butenyl ethyl ether 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: 48.0%

: 929-05-5
1-ethoxybut-1-ene

: 1528-20-7
(E)-1-ethoxybut-1-ene

Guidance literature:: With ethene; Mo(N^iPrPh)-(CHCMe₂Ph)(Me₂Pyrr)(OBitet); at 22 ℃; for 2h; under 3040.2 Torr; stereoselective reaction; Inert atmosphere;
DOI:10.1021/ja205002v