(1R,2S)-Naphthalene 1,2-oxide

Base Information

Chemical Name:(1R,2S)-Naphthalene 1,2-oxide
CAS No.:73136-20-6
Molecular Formula:C₁₀H₈O
Molecular Weight:144.173
Hs Code.:
DSSTox Substance ID:DTXSID901264379
Nikkaji Number:J442.342I
Wikidata:Q27115739
Metabolomics Workbench ID:54900

Synonyms:(1R,2S)-Naphthalene 1,2-oxide;(1R,2S)-Naphthalene epoxide;73136-20-6;(1aS,7bR)-1a,7b-dihydronaphtho[1,2-b]oxirene;(+)-1R,2S-Naphthalene epoxide;(+)-(1R,2S)-Naphthalene epoxide;(1R,2S)-1,2-epoxy-1,2-dihydronaphthalene;Naphth(1,2-b)oxirene, 1a,7b-dihydro-, (1aS,7bR)-;SCHEMBL12189732;CHEBI:33998;DTXSID901264379;(1aS,7bR)-1a,7b-Dihydronaphth[1,2-b]oxirene;Q27115739

Suppliers and Price of (1R,2S)-Naphthalene 1,2-oxide

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 0 raw suppliers

Chemical Property of (1R,2S)-Naphthalene 1,2-oxide

Chemical Property:

Vapor Pressure:0.0162mmHg at 25°C
Boiling Point:264.1°Cat760mmHg
Flash Point:109.4°C
Density:1.207g/cm³
XLogP3:1.8
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:0
Exact Mass:144.057514874
Heavy Atom Count:11
Complexity:197

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C2C3C(O3)C=CC2=C1
Isomeric SMILES:C1=CC=C2[C@@H]3[C@@H](O3)C=CC2=C1

Technology Process of (1R,2S)-Naphthalene 1,2-oxide

There total 29 articles about (1R,2S)-Naphthalene 1,2-oxide 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%

: 447-53-0
1,2-Dihydronaphthalene

: 17180-88-0,73136-20-6,84608-95-7,24825-00-1
(-)-(1S,2R)-naphthalene 1,2-oxide

Guidance literature:: With titanium(IV) isopropylate; (1R,2R)-N-[( hydroxy-3-phenyl)benzyl]-N’-[(2-hydroxy-3-phenyl)benzylidene]-1,2-diaminocyclohexane; dihydrogen peroxide; In dichloromethane; water; at 20 ℃; for 18h; Time; Concentration; optical yield given as %ee; diastereoselective reaction; Kinetics;
DOI:10.1002/adsc.200700601