5220-83-7

Basic information

• Product Name: 3-AMino-6-chloro-4-phenylcarbostyril
• Synonyms: 3-AMino-6-chloro-4-phenylcarbostyril;3-AMino-6-chloro-4-phenyl-2-quinolinone;3-AMino-6-chloro-4-phenylquinolin-2(1H)-one;3-amino-6-chloro-1,2-dihydro-2-oxo-4-phenylquinoline;3-amino-6-chloro-4-phenyl-1H-quinolin-2-one
• CAS NO: 5220-83-7
• Molecular Formula: C₁₅H₁₁ClN₂O
• Molecular Weight: 271
• Product Categories: Intermediates & Fine Chemicals;Pharmaceuticals
• Mol File: 5220-83-7.mol
• Article Data: 5

Chemical Properties

• Melting Point: 239-241 °C(Solv: ethanol (64-17-5))
• Boiling Point: 494.7±45.0 °C(Predicted)
• Appearance: /
• Density: 1.341±0.06 g/cm3(Predicted)
• Storage Temp.: 2-8°C
• Solubility: DMSO (Slightly), Methanol (Slightly)
• PKA: 9.76±0.70(Predicted)
• CAS DataBase Reference: 3-AMino-6-chloro-4-phenylcarbostyril(CAS DataBase Reference)
• NIST Chemistry Reference: 3-AMino-6-chloro-4-phenylcarbostyril(5220-83-7)
• EPA Substance Registry System: 3-AMino-6-chloro-4-phenylcarbostyril(5220-83-7)

Safety Data

• Hazardous Substances Data: 5220-83-7(Hazardous Substances Data)

Usage

Chemical Properties

Off-White Solid

Upstream product

• 4016-85-7 5-chloro-2-(chloroacetylamino)benzophenone 
• 80837-62-3 N-(2-Benzoyl-4-chloro-phenyl)-2-methanesulfonylamino-acetamide 
• 25759-97-1 1-(6-Chloro-2-oxo-4-phenyl-1,2-dihydro-quinolin-3-yl)-pyridinium; chloride 

Downstream Products

• 59163-16-5 6-chloro-2-methylsulfanyl-4-phenyl-quinolin-3-ylamine 
• 2854-15-1 3-acetylamino-6-chloro-4-phenyl-1H-quinolin-2-one 
• 136304-38-6 N-(6-chloro-1,2-dihydro-2-oxo-4-phenyl-3-quinolyl)-N'-(2,4-difluorophenyl)urea 
• 59318-12-6 di-morpholin-4-yl-phosphinic acid 3-amino-6-chloro-4-phenyl-quinolin-2-yl ester 
• 548446-48-6 [2-(6-chloro-1-methyl-2-oxo-4-phenyl-1,2-dihydroquinolin-3-ylcarbamoyl)-ethyl]-carbamic acid benzyl ester 
• 80837-68-9 6-chloro-3-methanosulfonamido-1-methyl-4-phenyl-quinolin-2-one 
• 2854-14-0 6-chloro-1-methyl-4-phenyl-3-(acetylamino)quinol-2-one 
• 2878-73-1 7-chloro-2-methyl-9-phenyl-[1,3]oxazolo[5,4-b]quinoline 
• 5220-02-0 3-amino-6-chloro-1,2-dihydro-1-methyl-2-oxo-4-phenylquinoline 
• 80837-67-8 6-chloro-3-methanosulfonamido-4-phenyl-1H-quinolin-2-one 
• 548446-45-3 2-acetamido-2-acetoxy-6-chloro-4-phenyl-quinoline 

Relevant articles and documents

Synthesis and in vitro anti-hepatitis B virus activities of 4-aryl-6-chloro-quinolin-2-one and 5-aryl-7-chloro-1,4-benzodiazepine derivatives

A series of 4-aryl-6-chloro-quinolin-2-ones and 5-aryl-7-chloro-1,4-benzodiazepine were synthesized and assayed for their in vitro anti-hepatitis B virus activities and cytotoxicities for the first time. Some of the tested compounds were active against HBsAg and HBeAg secretion in Hep G2.2.15 cells. Compound 5c showed IC50 of 0.074 and 0.449 mM on HBsAg and HBeAg secretions, respectively, which were 10 times higher than that of its analog 4c and led to better selective index (SI) values (SI = 23.2 and 3.4, respectively).

On the synthesis of 3-amino-4-aryl-2(1H)-quinolinones

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QUINAZOLINES AND 1,4-BENZODIAZEPINES. XXII. A REARRANGEMENT OF

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