2--4-(benzyloxy)-1-bromonaphthalene

Base Information

Chemical Name:2--4-(benzyloxy)-1-bromonaphthalene
CAS No.:161361-90-6
Molecular Formula:C₂₅H₂₆BrNO₃
Molecular Weight:468.39
Hs Code.:

2-<N-allyl-N-(tert-butyloxycarbonyl)amino>-4-(benzyloxy)-1-bromonaphthalene

Synonyms:2--4-(benzyloxy)-1-bromonaphthalene

Suppliers and Price of 2--4-(benzyloxy)-1-bromonaphthalene

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 2--4-(benzyloxy)-1-bromonaphthalene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2--4-(benzyloxy)-1-bromonaphthalene

There total 1 articles about 2--4-(benzyloxy)-1-bromonaphthalene 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: 32.0%

: 122745-37-3
2-((tert-Butyloxycarbonyl)amino)-4-(benzyloxy)-1-bromonaphthalene

: 106-95-6
allyl bromide

: 161361-90-6
2--4-(benzyloxy)-1-bromonaphthalene

Guidance literature:: With sodium hydride;
DOI:10.1021/jm020526p

Reference yield: 84.0%

: 161361-90-6
2--4-(benzyloxy)-1-bromonaphthalene

: 550356-45-1
tert-butyl 5-(benzyloxy)-1-methyl-1,2-dihydro-3H-benzo[e]indole-3-carboxylate

Guidance literature:: With 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; In benzene; for 1h; Heating;
DOI:10.1021/jm020526p

Reference yield:

: 161361-90-6
2--4-(benzyloxy)-1-bromonaphthalene

: 2--4-(benzyloxy)-1-bromonaphthalene

Guidance literature:: With sodium hydroxide; 9-borabicyclo[3.3.1]nonane dimer; dihydrogen peroxide; Yield given. Multistep reaction; 1.) THF, 25 deg C, 16 h, 2.) THF, from 0 to 60 deg C, 2.5 h;