Quinoline-8-carboxaldehyde, thiosemicarbazone

Base Information

Chemical Name:Quinoline-8-carboxaldehyde, thiosemicarbazone
CAS No.:3652-39-9
Molecular Formula:C₁₁H₁₀N₄S
Molecular Weight:230.293
Hs Code.:
Mol file:3652-39-9.mol

Synonyms:BRN 0178613;Quinoline-8-carboxaldehyde, thiosemicarbazone;4-21-00-04047 (Beilstein Handbook Reference);3652-39-9;8-Formylquinoline thiosemicarbazone;Hydrazinecarbothioamide, 2-(8-quinolinylmethylene)-;[(E)-8-quinolylmethyleneamino]thiourea;LS-141375

Suppliers and Price of Quinoline-8-carboxaldehyde, thiosemicarbazone

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
QUINOLINE-8-CARBOXALDEHYDE THIOSEMICARBAZONE 95.00%
5MG
$ 499.31

Total 4 raw suppliers

Chemical Property of Quinoline-8-carboxaldehyde, thiosemicarbazone

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Boiling Point:432.6°Cat760mmHg
Flash Point:215.4°C
PSA：95.39000
Density:1.33g/cm³
LogP:2.49310
XLogP3:1.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:230.06261751
Heavy Atom Count:16
Complexity:279

Purity/Quality:

95% ^*data from raw suppliers

QUINOLINE-8-CARBOXALDEHYDE THIOSEMICARBAZONE 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C(=C1)C=NNC(=S)N)N=CC=C2
Isomeric SMILES:C1=CC2=C(C(=C1)/C=N/NC(=S)N)N=CC=C2

Technology Process of Quinoline-8-carboxaldehyde, thiosemicarbazone

There total 1 articles about Quinoline-8-carboxaldehyde, thiosemicarbazone 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: 70.0%