1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

Base Information

Chemical Name:1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene
CAS No.:1372769-09-9
Molecular Formula:C₁₈H₁₇NO₂
Molecular Weight:279.338
Hs Code.:

Synonyms:1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

Suppliers and Price of 1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

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 1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

There total 1 articles about 1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene 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: 96.0%

: 506-68-3
bromocyane

: 1280721-99-4
C₁₇H₁₈O₂

: 1372769-09-9
1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

Guidance literature:: With triethylamine; In diethyl ether; hexane; at 0 ℃; for 3h; Inert atmosphere;
DOI:10.1021/ja301375c

Reference yield: 60.0%

: 1372769-09-9
1-{2-[(benzyloxy)methyl]allyl}-2-cyanatobenzene

: 1372769-22-6
2-(2-((benzoxy)methyl)-2,3-dihydrobenzofuran-2-yl)acetonitrile

Guidance literature:: With tris-(dibenzylideneacetone)dipalladium⁽⁰⁾; triphenylborane; 4,5-bis(diphenylphos4,5-bis(diphenylphosphino)-9,9-dimethylxanthenephino)-9,9-dimethylxanthene; In tetrahydrofuran; dodecane; at 80 ℃; for 2h; chemoselective reaction;
DOI:10.1021/ja301375c