10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime

Base Information

Chemical Name:10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime
CAS No.:34144-41-7
Molecular Formula:C19H19N3O3
Molecular Weight:337.3725
Hs Code.:

Synonyms:BRN 1162975;10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime;5H-Benzo(4,5)cyclohepta(1,2-b)pyridin-5-one, 10,11-dihydro-, O-(morpholinocarbonyl)oxime;C19H19N3O3;34144-41-7;LS-33794

Suppliers and Price of 10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime

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 10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:499.5°Cat760mmHg
Flash Point:255.9°C
Density:1.32g/cm³
XLogP3:2.6
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:337.14264148
Heavy Atom Count:25
Complexity:504

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CC2=C(C=CC=N2)C(=NOC(=O)N3CCOCC3)C4=CC=CC=C41
Isomeric SMILES:C1CC2=C(C=CC=N2)/C(=N\OC(=O)N3CCOCC3)/C4=CC=CC=C41

Technology Process of 10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime

There total 1 articles about 10,11-Dihydro-5H-benzo(4,5)cyclohepta(1,2-b)pyrid-5-one O-(morpholinocarbonyl)oxime 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: