6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline

Base Information

Chemical Name:6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline
CAS No.:81892-50-4
Molecular Formula:C₁₁H₁₂BrN₃O₂
Molecular Weight:298.139
Hs Code.:
Mol file:81892-50-4.mol

Synonyms:6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline;81892-50-4;6-Bromo-3,4-dihydro-4-(hydroxyimino)-N-methyl-1(2H)-quinolinecarboxamide;1(2H)-Quinolinecarboxamide, 6-bromo-3,4-dihydro-4-(hydroxyimino)-N-methyl-;(4Z)-6-Bromo-4-(hydroxyimino)-N-methyl-3,4-dihydro-1(2H)-quinolinecarboxamide;C11-H12-Br-N3-O2;SCHEMBL11141236;LS-141380

Suppliers and Price of 6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline

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

American Custom Chemicals Corporation
1(2H)-QUINOLINECARBOXAMIDE, 6-BROMO-3,4-DIHYDRO-4-(HYDROXYIMINO)-N-MET HYL- 95.00%
5MG
$ 503.56

Total 3 raw suppliers

Chemical Property of 6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline

Chemical Property:

Vapor Pressure:8.81E-13mmHg at 25°C
Boiling Point:546.6°C at 760 mmHg
Flash Point:284.4°C
PSA：68.42000
Density:1.66g/cm³
LogP:2.44630
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:0
Exact Mass:297.01129
Heavy Atom Count:17
Complexity:335

Purity/Quality:: 1(2H)-QUINOLINECARBOXAMIDE, 6-BROMO-3,4-DIHYDRO-4-(HYDROXYIMINO)-N-MET HYL- 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CNC(=O)N1CCC(=NO)C2=C1C=CC(=C2)Br
Isomeric SMILES:CNC(=O)N1CC/C(=N/O)/C2=C1C=CC(=C2)Br

Technology Process of 6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline

There total 1 articles about 6-Bromo-4-oximino-1-methylcarbamoyl-1,2,3,4-tetrahydroquinoline 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: