3-(2-Bromo-1-ethoxyethoxy)cyclohexene

Base Information

Chemical Name:3-(2-Bromo-1-ethoxyethoxy)cyclohexene
CAS No.:85710-98-1
Molecular Formula:C10H17BrO2
Molecular Weight:249.148
Hs Code.:
DSSTox Substance ID:DTXSID20527365
Nikkaji Number:J1.175.376K

Synonyms:3-(2-bromo-1-ethoxyethoxy)cyclohexene;85710-98-1;DTXSID20527365;3-(2-bromo-1-ethoxyethoxy)-1-cyclohexene;3-(2-Bromo-1-ethoxyethoxy)cyclohex-1-ene

Suppliers and Price of 3-(2-Bromo-1-ethoxyethoxy)cyclohexene

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of 3-(2-Bromo-1-ethoxyethoxy)cyclohexene

Chemical Property:

XLogP3:2.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:248.04119
Heavy Atom Count:13
Complexity:159

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCOC(CBr)OC1CCCC=C1

Technology Process of 3-(2-Bromo-1-ethoxyethoxy)cyclohexene

There total 1 articles about 3-(2-Bromo-1-ethoxyethoxy)cyclohexene 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:

: 2983-26-8
1,2-dibromoethyl ethyl ether

: 822-67-3
Cyclohex-2-enol

: 85710-98-1
1-Bromo-2-ethoxy-2-(1-cyclhexene-3-oxy)ethane

Guidance literature:: DOI:10.1021/ja00349a082

Reference yield:

: 85710-98-1
1-Bromo-2-ethoxy-2-(1-cyclhexene-3-oxy)ethane

: 6051-03-2,24871-12-3,27345-71-7,43119-27-3,61248-46-2,74708-14-8,74708-15-9,74708-16-0,74741-45-0
cis-hexahydrobenzofuran-2(3H)-one

Guidance literature:: Multi-step reaction with 2 steps

1: 83 percent / Cr₂(OAc)4(H₂O)2, ethylenediamine, LiAlH₄ / tetrahydrofuran / 1 h / Ambient temperature

2: 71 percent / Jones-reagent / acetone / 0.25 h / 0 °C

With lithium aluminium tetrahydride; chromium(II) diacetate dimer; Jones-reagent; ethylenediamine; In tetrahydrofuran; acetone;
DOI:10.1016/S0040-4020(01)81285-0

Reference yield:

: 85710-98-1
1-Bromo-2-ethoxy-2-(1-cyclhexene-3-oxy)ethane

: ((1R,6S)-6-Hydroxy-cyclohex-2-enyl)-acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: 70 percent / chloro(pyridino)bis-(dimethylglyoximato)cobalt(I)

3: Jones reagent

With jones reagent; (pyridine)Co(dimethylglyoxime)2Cl;
DOI:10.1016/S0040-4039(00)84513-X