6-Fluoro-4-oximino-1-dimethylcarbamoyl-1,2,3,4-tetrahydroquinoline

Base Information

Chemical Name:6-Fluoro-4-oximino-1-dimethylcarbamoyl-1,2,3,4-tetrahydroquinoline
CAS No.:81892-51-5
Molecular Formula:C₁₂H₁₄FN₃O₂
Molecular Weight:251.26
Hs Code.:
Mol file:81892-51-5.mol

Synonyms:6-Fluoro-4-oximino-1-dimethylcarbamoyl-1,2,3,4-tetrahydroquinoline;81892-51-5;1(2H)-Quinolinecarboxamide, 6-fluoro-3,4-dihydro-4-(hydroxyimino)-N,N-dimethyl-;6-Fluoro-3,4-dihydro-4-(hydroxyimino)-N,N-dimethyl-1(2H)-quinolinecarboxamide;C12H14FN3O2;C12-H14-F-N3-O2;SCHEMBL11141587;LS-141446

Suppliers and Price of 6-Fluoro-4-oximino-1-dimethylcarbamoyl-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
6-FLUORO-3,4-DIHYDRO-4-(HYDROXYIMINO)-N,N-DIMETHYL-1(2H)-QUINOLINECARB OXAMIDE 95.00%
5MG
$ 500.47

Total 3 raw suppliers

Chemical Property of 6-Fluoro-4-oximino-1-dimethylcarbamoyl-1,2,3,4-tetrahydroquinoline

Chemical Property:

Vapor Pressure:1.8E-07mmHg at 25°C
Boiling Point:410.4°C at 760 mmHg
Flash Point:202°C
PSA：56.14000
Density:1.31g/cm³
LogP:1.96070
XLogP3:1.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:0
Exact Mass:251.10700486
Heavy Atom Count:18
Complexity:359

Purity/Quality:: 6-FLUORO-3,4-DIHYDRO-4-(HYDROXYIMINO)-N,N-DIMETHYL-1(2H)-QUINOLINECARB OXAMIDE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

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

Technology Process of 6-Fluoro-4-oximino-1-dimethylcarbamoyl-1,2,3,4-tetrahydroquinoline

There total 1 articles about 6-Fluoro-4-oximino-1-dimethylcarbamoyl-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: