3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

Base Information

Chemical Name:3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane
CAS No.:73752-15-5
Molecular Formula:C₈H₁₂O₂
Molecular Weight:140.182
Hs Code.:
Mol file:73752-15-5.mol

Synonyms:1-(Epoxyethyl)-3,4-epoxycyclohexane polymer;3-(1,2-Epoxyethyl)-7-oxabicyclo(4.1.0)heptane polymer;4-Oxiranyl-1,2-epoxycyclohexane polymer;4-Vinylcyclohexene diepoxide polymer;4-Vinylcyclohexene dioxide homopolymer;7-Oxabicyclo(4.1.0)heptane, 3-oxiranyl-, homopolymer;Araldite dy 032

Suppliers and Price of 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

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 3 raw suppliers

Chemical Property of 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

Chemical Property:

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

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Technology Process of 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane

There total 14 articles about 3-(oxiran-2-yl)-7-oxabicyclo[4.1.0]heptane 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: 88.0%

: 100-40-3
4-ethenylcyclohexene

: 106-87-6,73752-15-5
4-vinylcyclohexene dioxide

Guidance literature:: With 2,2,2-Trifluoroacetophenone; dihydrogen peroxide; In acetonitrile; tert-butyl alcohol; at 20 ℃; for 1h; Green chemistry;
DOI:10.1021/jo5003938

Reference yield: 74.0%

: 100-40-3
4-ethenylcyclohexene

: 106-87-6,73752-15-5
4-vinylcyclohexene dioxide

: C₈H₁₂O

Guidance literature:: With C₂₀H₂₆FeN₄⁽²⁺⁾*2CF₃O₃S^(1-); dihydrogen peroxide; acetic acid; In acetonitrile; at 0 ℃; for 0.166667h; regioselective reaction;
DOI:10.1002/ejic.201500213

Reference yield: 2.5%

: 632-21-3
1,1,3,3-tetrachloropropanone

: 100-40-3
4-ethenylcyclohexene

: 106-87-6,73752-15-5
4-vinylcyclohexene dioxide

: 106-86-5
1,2-Epoxy-4-vinylcyclohexane

: 5116-65-4
7,8-Epoxy-1-Cyclohexene

: 78950-58-0
tetrachloroacetone hydrate

Guidance literature:: With disodium hydrogenphosphate; dihydrogen peroxide; In chloroform; for 24h; Ambient temperature;
DOI:10.1016/S0040-4039(01)93284-8