6019-43-8

Basic information

• Product Name: 2-Quinolinecarboxamide, N-(phenylmethyl)-
• CAS NO: 6019-43-8
• Molecular Formula: C17H14N2O
• Molecular Weight: 262.311
• Mol File: 6019-43-8.mol
• Article Data: 12

Chemical Properties

• CAS DataBase Reference: 2-Quinolinecarboxamide, N-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Quinolinecarboxamide, N-(phenylmethyl)-(6019-43-8)
• EPA Substance Registry System: 2-Quinolinecarboxamide, N-(phenylmethyl)-(6019-43-8)

Safety Data

• Hazardous Substances Data: 6019-43-8(Hazardous Substances Data)

Upstream product

• 4491-33-2 ethyl quinoline-2-carboxylate 
• 100-46-9 benzylamine 
• 2005-43-8 2-bromoquinoline 
• 13463-40-6 iron pentacarbonyl 
• 91-22-5 quinoline 
• 6345-08-0 2-(benzylamino)-2-oxoacetic acid 
• 613-53-6 2-tribromomethyl-quinoline 
• 93-10-7 quinoline-2-carboxylic acid 
• 612-62-4 2-Chloroquinoline 
• 13939-06-5 molybdenum hexacarbonyl 
• 50342-01-3 quinolin-2-ylcarbonyl chloride 

Downstream Products

• 1443005-42-2 N-(4-chlorobenzoyl)-N-benzylquinoline-2-carboxamide 
• 42116-44-9 N-tert-butoxycarbonylbenzylamine 
• 351900-21-5 benzyl-(quinoline-2-carbonyl)-carbamic acid tert-butyl ester 
• 1610539-75-7 (E)-methyl 2-(2-benzyl-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-b]quinolin-1-ylidene)acetate 
• 1610539-83-7 methyl 2-(2-benzyl-3-oxo-2,3-dihydro-1H-pyrrolo[3,4-b]quinolin-1-yl)acetate 

Relevant articles and documents

Silver-catalyzed direct C-H oxidative carbamoylation of quinolines with oxamic acids

A silver-catalyzed efficient and direct C-H carbamoylation of quinolines with oxamic acids to access carbamoylated quinolines has been developed through oxidative decarboxylation reaction. The reaction proceeds smoothly over a broad range of substrates wi

Triphenylphosphine-catalysed amide bond formation between carboxylic acids and amines

Unactivated carboxylic acids and amines undergo organocatalytic Ph 3P/CCl4-mediated amide bond formation by employing in situ reduction of triphenylphosphine oxide to triphenylphosphine in the presence of diethoxymethylsilane and bis(4-nitrophenyl)phosphate. the Partner Organisations 2014.

Novel method of synthesizing various five membered heterocycles from an aryl tribromomethyl group

Synthesis of five membered heterocycles from an aryl tribromomethyl functional group is discussed. Exposing a tribromomethyl group to subsequent nucleophilic attacks by a 1,2-di-nucleophilic species promotes the cyclization of five membered heterocycles. Such heterocycles as oxadiazoles, thiadiazole, benzimidazole, benzothioazole, and benzoxazole were synthesized in moderate to good yields. Supplemental materials are available for this article. Go to the publisher's online edition of Synthetic Communications to view the free supplemental file.