148315-27-9

Basic information

• Product Name: 2-Quinolinecarboxylic acid, pentafluorophenyl ester
• CAS NO: 148315-27-9
• Molecular Formula: C16H6F5NO2
• Molecular Weight: 339.221
• Mol File: 148315-27-9.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2-Quinolinecarboxylic acid, pentafluorophenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Quinolinecarboxylic acid, pentafluorophenyl ester(148315-27-9)
• EPA Substance Registry System: 2-Quinolinecarboxylic acid, pentafluorophenyl ester(148315-27-9)

Safety Data

• Hazardous Substances Data: 148315-27-9(Hazardous Substances Data)

Upstream product

• 93-10-7 quinoline-2-carboxylic acid 
• 771-61-9 2,3,4,5,6-pentafluorophenol 

Downstream Products

• 778587-26-1 N-cyclohexyl-N-methylquinoline-2-carboxamide 
• 586371-25-7 N-ethyl-N-phenylquinoline-2-carboxamide 
• 1527472-56-5 N-(4-(4-(dimethylamino)benzoyl)phenyl)-N-methylquinoline-2-carboxamide 

Relevant articles and documents

Aminolysis of aryl ester using tertiary amine as amino donor via c-o and c-n bond activations

An aminolysis reaction between various aryl esters and inert tertiary amines by C-O and C-N bond activations has been developed for the selective synthesis of a broad scope of tertiary amides under neutral and mild conditions. The mechanism may undergo the two key steps of oxidative addition of acyl C-O bond in parent ester and C-N bond cleavage of tertiary amine via an iminium-type intermediate.

Ramoplanin derivatives possessing antibacterial activity

Novel ramoplanin derivatives are disclosed. These ramoplanin derivatives exhibit antibacterial activity. As the compounds of the subject invention exhibit potent activities against gram positive bacteria, they are useful antimicrobial agents. Methods of synthesis and of use of the compounds are also disclosed.