1,2-Epoxyoctahydropentalene

Base Information

Chemical Name:1,2-Epoxyoctahydropentalene
CAS No.:6567-98-2
Molecular Formula:C₈H₁₂O
Molecular Weight:124.183
Hs Code.:
European Community (EC) Number:229-489-0
DSSTox Substance ID:DTXSID60970790
Nikkaji Number:J225.190F
Mol file:6567-98-2.mol

Synonyms:1,2-Epoxyoctahydropentalene;6567-98-2;Octahydropentaleno[1,2-b]oxirene;EINECS 229-489-0;OCTAHYDROPENTALENO(1,2-B)OXIRENE;55449-70-2;SCHEMBL9821322;DTXSID60970790;Octahydropentaleno[1,2-b]oxirene #;Pentaleno(1,2-b)oxirene, octahydro-;Pentaleno[1,2-b]oxirene, octahydro-, (1a.alpha.,1b.alpha.,4a.beta.,5a.alpha.)-;Pentaleno[1,2-b]oxirene, octahydro-, (1a.alpha.,1b.beta.,4a.alpha.,5a.alpha.)-

Suppliers and Price of 1,2-Epoxyoctahydropentalene

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 5 raw suppliers

Chemical Property of 1,2-Epoxyoctahydropentalene

Chemical Property:

Vapor Pressure:0.997mmHg at 25°C
Boiling Point:184.6°C at 760 mmHg
Flash Point:45.7°C
PSA：0.00000
Density:1.101g/cm³
LogP:0.00000
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:124.088815002
Heavy Atom Count:9
Complexity:144

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CC2CC3C(C2C1)O3

Technology Process of 1,2-Epoxyoctahydropentalene

There total 8 articles about 1,2-Epoxyoctahydropentalene 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: 59.0%

: 930-99-4
(3aS,6aS)-1,2,3,3a,4,6a-Hexahydro-pentalene

: 6567-98-2,24454-41-9,24454-42-0,55449-70-2,55449-71-3
(1bR,4aR)-Octahydro-1-oxa-cyclopropa[a]pentalene

Guidance literature:: With 1-methyl-pyrrolidin-2-one; 18-crown-6 ether; dihydrogen peroxide; sodium carbonate; trichlorophosphate; In dichloromethane; 1) -20 deg C, 1h, 2) -20 deg C, to 20 deg C;
DOI:10.1021/jo00001a095

Reference yield: 53.0%

: 5549-09-7
bicyclo[3.3.0]oct-2-ene

: 6567-98-2,24454-41-9,24454-42-0,55449-70-2,55449-71-3
(+/-)-2β,3β-epoxy-1α,2β,3β,5α-bicyclo[3.3.0]oct-2-eneoxirane

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In chloroform; for 2h; Heating;
DOI:10.1021/jo9615155

Reference yield:

: 930-99-4
(3aS,6aS)-1,2,3,3a,4,6a-Hexahydro-pentalene

: 6567-98-2,24454-41-9,24454-42-0,55449-70-2,55449-71-3
(+/-)-2β,3β-epoxy-1α,2β,3β,5α-bicyclo[3.3.0]oct-2-eneoxirane

: 6567-98-2,24454-41-9,24454-42-0,55449-70-2,55449-71-3
endo-2,3-Epoxy-cis-bicyclo<3.3.0>octan; endo-cis-Bicyclo<3.3.0>octen-(2)-oxid

Guidance literature:: With sodium hydroxide; N-Bromosuccinimide; Yield given. Multistep reaction. Yields of byproduct given; 1) DMSO-H₂O, room temp., 2) H₂O, room temp.;
DOI:10.1016/0040-4039(84)80040-4