58668-43-2

Basic information

• Product Name: Benzoic acid, 2-[(2-pyridinylcarbonyl)amino]-
• CAS NO: 58668-43-2
• Molecular Formula: C13H10N2O3
• Molecular Weight: 242.234
• Mol File: 58668-43-2.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: Benzoic acid, 2-[(2-pyridinylcarbonyl)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzoic acid, 2-[(2-pyridinylcarbonyl)amino]-(58668-43-2)
• EPA Substance Registry System: Benzoic acid, 2-[(2-pyridinylcarbonyl)amino]-(58668-43-2)

Safety Data

• Hazardous Substances Data: 58668-43-2(Hazardous Substances Data)

Upstream product

• 98-98-6 2-Picolinic acid 
• 134-20-3 2-carbomethoxyaniline 
• 29745-44-6 pyridine-2-carbonyl chloride 
• 118-92-3 anthranilic acid 
• 69873-67-2 methyl 2-[(pyridinecarbonyl)amino]benzoate 

Downstream Products

• 110018-84-3 Cu(NC₅H₄CONHC₆H₄CO₂)(NC₅H₄CONHC₆H₄CO₂H)NO₃ 
• 110018-77-4 Cu(NC₅H₄CONHC₆H₄CO₂H)2Cl₂*C₂H₅OH 
• 110018-75-2 Co(NC₅H₄CONHC₆H₄CO₂H)2Cl₂*C₂H₅OH 
• 110018-82-1 Zn(NC₅H₄CONHC₆H₄CO₂H)2(NO₃)2 
• 110018-78-5 Co(NC₅H₄CONHC₆H₄CO₂H)2(NCS)2 
• 110018-79-6 Ni(NC₅H₄CONHC₆H₄CO₂H)2(NCS)2 
• 110018-81-0 Ni(NC₅H₄CONHC₆H₄CO₂H)2(NO₃)2 
• 110018-80-9 Co(NC₅H₄CONHC₆H₄CO₂H)2(NO₃)2 
• 110037-08-6 Ni(NC₅H₄CONHC₆H₄CO₂H)2Cl₂*C₂H₅OH*H₂O 

Relevant articles and documents

Ru-based complexes as heterogeneous potential catalysts for the amidation of aldehydes and nitriles in neat water

Five novel heterogeneous mononuclear complex-anchored Ru(III) have been efficiently sono-synthesized and characterized by utilizing several analytical techniques. The assembled complexes could be utilized as effective, robust and recyclable (up to eight consecutive runs) catalysts for one-pot transformation of a vast array of nitriles and aldehydes to primary amides in H2O under aerobic conditions. Moreover, some unreported di- and tetra-amide derivatives were obtained also under the optimal conditions. The results of ICP/OES analysis demonstrated that there is no detected leaching of the recycled catalyst, which suggests the real heterogeneity of the present protocol. The present Ru-complexes exhibited superiority compared to other reported catalysts for amide preparation in terms of low catalyst load, short reaction time, low operating temperature, no hazardous additives required, and high values of TON (990) and TOF (1980 h11).

Synthesis and biological properties of selected 2-aryl-4(3H)-quinazolinones

A series of 2-aryl-4(3H)quinazolinones were prepared as parent systems of rutaecarpine and luoitonin A and their biological properties (cytotoxicity and COX-2 inhibitory activity) were evaluated.