N-Phenylquinoline-4-amine

N-Phenylquinoline-4-amine Suppliers list
Company Name: Shanghai Changer Pharmaceutical Technology Co. Ltd.  
Tel: 15921595598
Email: qd.yu@pharmachanger.com
Products Intro: Product Name:n-phenylquinolin-4-amine
CAS:30696-07-2
Purity:98% Package:1G;5G;10G;25G;100G;250G;500G;1KG
Company Name: Shanghai Haohong Pharmaceutical Co., Ltd.  
Tel: 4008210725 4008210725
Email: malulu@leyan.com
Products Intro: Product Name:N-phenylquinolin-4-amine
CAS:30696-07-2
Purity:98%
Company Name: Bide Pharmatech Ltd.  
Tel: 400-1647117 15221909166
Email: product02@bidepharm.com
Products Intro: Product Name:N-Phenylquinolin-4-amine
CAS:30696-07-2
Purity:97% Package:100mg;250mg;1g Remarks:BD604489
Company Name: Bide Pharmatech Ltd.  
Tel: 400-6005915
Email: sales@picasso-e.com
Products Intro: Product Name:N-Phenylquinolin-4-amine
CAS:30696-07-2
Purity:97% Package:100mg;250mg;1g
Company Name: Hepharma Biology And Technology CO.,LTD.  
Tel: 187-26307739 18726307739
Email: waimaobu@hepharma.cn
Products Intro: Product Name:N-Phenylquinolin-4-amine
CAS:30696-07-2
Purity:98%;99% Package:按要求包装
N-Phenylquinoline-4-amine Basic information
Product Name:N-Phenylquinoline-4-amine
Synonyms:4-Anilinoquinoline;N-Phenylquinoline-4-amine;n-phenylquinolin-4-aMine;phenyl-quinolin-4-yl-amine;4-Quinolinamine, N-phenyl-
CAS:30696-07-2
MF:C15H12N2
MW:220.27
EINECS:
Product Categories:
Mol File:30696-07-2.mol
N-Phenylquinoline-4-amine Structure
N-Phenylquinoline-4-amine Chemical Properties
Melting point 230 °C
Boiling point 380.2±17.0 °C(Predicted)
density 1.204±0.06 g/cm3(Predicted)
pka6.70±0.13(Predicted)
Safety Information
HS Code 2933998090
MSDS Information
N-Phenylquinoline-4-amine Usage And Synthesis
SynthesisN-phenylquinolin-4-amine was prepared by adding aniline to 4-chloroquinoline ethanol solution under microwave irradiation at 165°C.
Experiment steps:To a solution of 4-chloroquinoline (350 mg, 2.14 mmol) in ethanol (3 ml), aniline (996 mg, 10.7 mmol) was added and the mixture was reacted at 165 °C for 3 hours under microwave radiation. The reaction mixture was concentrated in vacuo, aqueous sodium carbonate (25 ml) was added and this was then extracted using dichloromethane (3×30 ml). The organic extracts were collected, dried using magnesium sulphate, concentrated in vacuo and the resulting residue was purified by flash column chromatography eluting with 2% methanol in dichloromethane to give N-phenylquinolin-4-amine as a colourless solid (42 mg, 9%).
N-Phenylquinoline-4-amine Preparation Products And Raw materials
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