108835-25-2

Upstream product

• 4053-44-5 5-(hydroxymethyl)-8-hydroxyquinoline 
• 100-44-7 benzyl chloride 
• 4053-45-6 5-chloromethyl-8-hydroxyquinoline hydrochloride 
• 148-24-3 8-quinolinol 
• 100-39-0 benzyl bromide 

Downstream Products

• 108835-26-3 8-(benzyloxy)-5-(hydroxymethyl)quinoline N-oxide 
• 200285-24-1 8-benzyloxy-5-formylquinoleine 
• 128232-11-1 5-<2-<<1-(4-iodophenyl)-2-methylprop-2-yl>amino>-1-hydroxyethyl>-8-hydroxycarbostyril 
• 108835-37-6 5-<2-<<3-<4-(bromoacetamido)phenyl>-2-methylprop-2-yl>amino>-1-hydroxyethyl>-8-hydroxycarbostyril hydrobromide 
• 128232-10-0 8-(benzyloxy)-5-<2-<<1-(4-nitrophenyl)-2-methylprop-2-yl>amino>-1-hydroxyethyl>carbostyril 
• 128232-09-7 8-Benzyloxy-5-{1-hydroxy-2-[2-(4-iodo-phenyl)-1,1-dimethyl-ethylamino]-ethyl}-1H-quinolin-2-one 
• 128232-08-6 8-(benzyloxy)-5-<2-<(1-phenyl-2-methylprop-2-yl)amino>-1-hydroxyethyl>carbostyril 
• 120551-46-4 5-{2-[2-(4-Amino-phenyl)-1,1-dimethyl-ethylamino]-1-hydroxy-ethyl}-8-hydroxy-1H-quinolin-2-one 
• 112281-28-4 8-benzyloxy-5-(epoxyethyl)-(1H)-quinolin-2-one 
• 108835-27-4 8-(benzyloxy)quinoline-5-carboxaldehyde N-oxide 
• 67449-41-6 8-hydroxy-5-<2-<(1-phenyl-2-methylprop-2-yl)amino>-1-hydroxyethyl>carbostyril 
• 66546-38-1 8-(benzyloxy)carbostyril-5-carboxaldehyde 

Relevant academic research and scientific papers

Synthesis of 5-alkyl-8-quinolinol

Synthesis of new 5-alkyl-8-quinolinol was described in order to obtain substituted copper 8-hydroxyquinolinate more soluble in organic solvents than unsubstituted one. The synthesis of copper complex is described and their solubility investigated in different solvents.

BETA-AGONIST CARBOSTYRIL DERIVATIVES, ASSAY METHOD AND PHARMACOLOGICAL COMPOSITION

Beta-agonist carbostyril derivatives having the formula STR1 wherein X may be the ortho, meta or para position and is selected from the group consisting of halogen, amino and substituted and unsubstituted lower alkanoylamino having from 1 to 6 carbon atom

Carbostyril Derivatives Having Potent β-Adrenergic Agonist Properties

Derivatives carrying a substituent in the para position of the phenyl group of 8-hydroxy-5--1-hydroxyethyl>carbostyril (10) were prepared and their effects on β-adrenoceptors evaluated in vitro.Unsubstituted compound