1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene

Base Information

Chemical Name:1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene
CAS No.:58851-64-2
Molecular Formula:C12H14O3
Molecular Weight:206.241
Hs Code.:
DSSTox Substance ID:DTXSID401209835
Wikidata:Q107889213
Mol file:58851-64-2.mol

Synonyms:58851-64-2;1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene;3,6-dimethoxy-1a,2,7,7a-tetrahydronaphtho[2,3-b]oxirene;starbld0033891;SCHEMBL9345145;XZIDAWSWGWZKOO-UHFFFAOYSA-N;DTXSID401209835;AKOS030255483;FT-0674995;2,3-epoxy-5,8-dimethoxy-1,2,3,4-tetrahydronaphthalene;6,7-epoxy-5,6,7,8-tetrahydro-1,4-dimethoxynaphthalene;6,7-epoxy-5,6,7,8-tetrahydro1,4-dimethoxynaphthalene;1a,2,7,7a-Tetrahydro-3,6-dimethoxynaphth[2,3-b]oxirene

Suppliers and Price of 1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene

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

TRC
1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene
1 g
$ 305.00

TRC
1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene
250mg
$ 95.00

Total 3 raw suppliers

Chemical Property of 1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene

Chemical Property:

PSA：30.99000
LogP:1.56980
Solubility.:Chloroform, Dichloromethane
XLogP3:1.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:206.094294304
Heavy Atom Count:15
Complexity:219

Purity/Quality:

99% ^*data from raw suppliers

1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=C2CC3C(O3)CC2=C(C=C1)OC
Uses 1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene can be used as leukotriene inhibitors.

Technology Process of 1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene

There total 7 articles about 1a,2,7,7a-Tetrahydro-3,6-dimethoxy-naphth[2,3-b]oxirene 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: 91.0%

: 55077-79-7
5,8-dimethoxy-1,4-dihydronaphthalene

: 58851-64-2
6,7-epoxy-5,6,7,8-tetrahydro-1,4-dimethoxynaphthalene

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 12h;
DOI:10.1081/SCC-200028508

Reference yield:

: 447-53-0
1,2-Dihydronaphthalene

: 58851-64-2
6,7-epoxy-5,6,7,8-tetrahydro-1,4-dimethoxynaphthalene

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In hexane; dichloromethane;

Reference yield:

: 106-51-4
p-benzoquinone

: 58851-64-2
6,7-epoxy-5,6,7,8-tetrahydro-1,4-dimethoxynaphthalene

Guidance literature:: Multi-step reaction with 2 steps

1: (i), (ii) /BRN= 635994/

2: 4-carboxy-peroxybenzoic acid / diethyl ether

With 4-carboxy-peroxybenzoic acid; In diethyl ether;
DOI:10.1002/ardp.19773100505