C₁₆H₁₇NO

Base Information

Chemical Name:C₁₆H₁₇NO
CAS No.:1229227-03-5
Molecular Formula:C₁₆H₁₇NO
Molecular Weight:239.317
Hs Code.:

Synonyms:C₁₆H₁₇NO

Suppliers and Price of C₁₆H₁₇NO

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 C₁₆H₁₇NO

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₁₆H₁₇NO

There total 2 articles about C₁₆H₁₇NO 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: 94.0%

: 24423-87-8,65194-03-8
3,4-dihydro-isoquinoline 2-oxide

: 5084-80-0
tri(4-tolyl)boroxine

: 1229227-03-5
C₁₆H₁₇NO

Guidance literature:: tri(4-tolyl)boroxine; With diethylzinc; In toluene; at 60 ℃; for 12h; Inert atmosphere;

3,4-dihydro-isoquinoline 2-oxide; With diethylzinc; [(1S)-1-((S)-1-methylpropyl)-(2-morpholin-4-ylethyl)]carbamic acid tert-butyl ester; In dichloromethane; toluene; at -30 - -20 ℃; for 24.25h; Inert atmosphere;

With methanol; In dichloromethane; toluene; at -20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol1004356

Reference yield: 79.0%

: 24423-87-8,65194-03-8
3,4-dihydro-isoquinoline 2-oxide

: 195062-57-8
p-tolylboronic pinacol ester

: 1229227-03-5
C₁₆H₁₇NO

Guidance literature:: p-tolylboronic pinacol ester; With diethylzinc; In toluene; at 70 ℃; for 12h; Inert atmosphere;

3,4-dihydro-isoquinoline 2-oxide; With diethylzinc; [(1S)-1-((S)-1-methylpropyl)-(2-morpholin-4-ylethyl)]carbamic acid tert-butyl ester; In dichloromethane; toluene; at -30 - -20 ℃; for 24.25h; Inert atmosphere;

With methanol; In dichloromethane; toluene; at -20 ℃; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol1004356