7,8-Bis(benzyloxy)-1,2-dihydronaphthalene

Base Information

Chemical Name:7,8-Bis(benzyloxy)-1,2-dihydronaphthalene
CAS No.:59516-85-7
Molecular Formula:C₂₄H₂₂O₂
Molecular Weight:342.437
Hs Code.:
DSSTox Substance ID:DTXSID40496004
Wikidata:Q82344531

Synonyms:59516-85-7;7,8-Bis(benzyloxy)-1,2-dihydronaphthalene;DTXSID40496004

Suppliers and Price of 7,8-Bis(benzyloxy)-1,2-dihydronaphthalene

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 1 raw suppliers

Chemical Property of 7,8-Bis(benzyloxy)-1,2-dihydronaphthalene

Chemical Property:

XLogP3:5.9
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:342.161979940
Heavy Atom Count:26
Complexity:434

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=C(C=C1)C=CC(=C2OCC3=CC=CC=C3)OCC4=CC=CC=C4

Technology Process of 7,8-Bis(benzyloxy)-1,2-dihydronaphthalene

There total 2 articles about 7,8-Bis(benzyloxy)-1,2-dihydronaphthalene 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:

: 65736-66-5
1,2,3,4-tetrahydro-5,6-dibenzyloxy-1-naphthalenol

: 59516-85-7
7,8-Dibenzyloxy-1,2-dihydro-1-naphthalin

Guidance literature:: With potassium hydrogensulfate;
DOI:10.1248/cpb.26.394

Reference yield:

: 59515-93-4
5,6-bis(benzyloxy)-3,4-dihydronaphthalen-1(2H)-one

: 59516-85-7
7,8-Dibenzyloxy-1,2-dihydro-1-naphthalin

Guidance literature:: Multi-step reaction with 2 steps

1: NaBH₄ / methanol

2: KHSO₄ / benzene

With sodium tetrahydroborate; potassium hydrogensulfate; In methanol; benzene;
DOI:10.1248/cpb.25.2917