36710-53-9

Basic information

• Product Name: 2-Phenylquinolin-3-amine
• Synonyms: 2-Phenylquinolin-3-amine
• CAS NO: 36710-53-9
• Molecular Formula: C₁₅H₁₂N₂
• Molecular Weight: 220.27
• Mol File: 36710-53-9.mol
• Article Data: 7

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-Phenylquinolin-3-amine(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Phenylquinolin-3-amine(36710-53-9)
• EPA Substance Registry System: 2-Phenylquinolin-3-amine(36710-53-9)

Safety Data

• Hazardous Substances Data: 36710-53-9(Hazardous Substances Data)

Upstream product

• 879721-09-2 2-phenyl-quinoline-3-carbonyl chloride 
• 17127-85-4 2-(2-isocyanophenyl)acetonitrile 
• 98-80-6 phenylboronic acid 
• 107468-25-7 3-azido-2-phenyl-3-quinoline 
• 78105-37-0 2-chloro-3-nitroquinoline 
• 5468-37-1 2-aminoacetophenone hydrochloride 
• 1018071-63-0 methyl 2-phenylquinoline-3-carboxylate 
• 4190-14-1 N-(2-oxo-2-phenylethyl)benzamide 
• 614-21-1 2-nitroacetophenone 
• 529-23-7 o-aminobenzaldehyde 
• 40312-83-2 2-cyclohexylamino-1-phenyl-ethanone 
• 70-11-1 α-bromoacetophenone 
• 91-56-5 indole-2,3-dione 
• 16883-69-5 N-phenacylpyridinium bromide 

Downstream Products

• 107468-31-5 3-Methoxy-2-phenyl-5H-benzo[e][1,4]diazepine 
• 107468-29-1 3-Methoxy-2-phenyl-3H-benzo[e][1,4]diazepine 
• 1207875-03-3 3-iodo-2-phenylquinoline 
• 102594-89-8 2-(2-phenylquinolin-3-yl)isoindoline-1,3-dione 
• 1643786-42-8 2-((2R,3R)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione 
• 1620395-12-1 2-((S,3S)-2-phenyl-1,2,3,4-tetrahydroquinolin-3-yl)isoindoline-1,3-dione 
• 876491-58-6 N-(2-phenyl-[3]quinolyl)-diacetamide 
• 107468-25-7 3-azido-2-phenyl-3-quinoline 
• 59280-67-0 3-chloro-2-phenyl quinoline 
• 5855-50-5 3-hydroxy-2-phenylquinoline 
• 5428-24-0 3-bromo-2-phenylquinoline 
• 500350-26-5 N-(2-phenyl-[3]quinolyl)-benzamide 
• 5463-89-8 2-phenyl-3-acetamidoquinoline 
• 1607448-81-6 tert-butyl 2-phenylquinolin-3-ylcarbamate 

Relevant articles and documents

Modular Synthesis of Polysubstituted Quinolin-3-amines by Oxidative Cyclization of 2-(2-Isocyanophenyl)acetonitriles with Organoboron Reagents

Polysubstituted quinolin-3-amines are vital structural motifs because of their broad biological activities as well as versatile transformational abilities. However, they are not easily accessible. We disclose a protocol with Mn(III) acetate as a mild one-

Synthesis of chiral exocyclic amines by asymmetric hydrogenation of aromatic quinolin-3-amines

Asymmetric hydrogenation of aromatic quinolin-3-amines was successfully developed with up to 94% enantiomeric excess (ee). Introduction of the phthaloyl moiety to the amino group is crucial to eliminate the inhibition effect caused by the substrate and pr

3-Pyridylnitrene, 2- and 4-pyrimidinylcarbenes, 3-quinolylnitrenes, and 4-quinazolinylcarbenes. Interconversion, ring expansion to diazacycloheptatetraenes, ring opening to nitrile ylides, and ring contraction to cyanopyrroles and cyanoindoles

Precursors of 3-pyridylnitrene and 2- and 4-pyrimidinylcarbenes all afford mixtures of 2- and 3-cyanopyrroles on flash vacuum thermolysis, but 3-cyanopyrroles are the first-formed products. 3-Quinolylnitrenes and 4-quinazolinylcarbenes similarly afford 3-cyanoindoles. 2-Pyrimidinylcarbenes rearrange to 3-pyridylnitrenes, but 4-pyrimidinylcarbenes and 4-quinazolinylcarbenes do not necessarily rearrange to the corresponding 3-pyridylnitrenes or 3-quinolylnitrenes. The ring contraction reactions are interpreted in terms of ring opening of either the nitrenes or the diazacycloheptatetraenes to nitrile ylides.