113416-61-8

Basic information

• Product Name: 2-Butenoic acid, 2-hydroxy-4-oxo-4-phenyl-
• CAS NO: 113416-61-8
• Molecular Formula: C10H8O4
• Molecular Weight: 192.171
• Mol File: 113416-61-8.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 2-Butenoic acid, 2-hydroxy-4-oxo-4-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 2-Butenoic acid, 2-hydroxy-4-oxo-4-phenyl-(113416-61-8)
• EPA Substance Registry System: 2-Butenoic acid, 2-hydroxy-4-oxo-4-phenyl-(113416-61-8)

Safety Data

• Hazardous Substances Data: 113416-61-8(Hazardous Substances Data)

Upstream product

• 88330-79-4 2-hydroxy-4-oxo-4-phenylbut-2-enoic acid ethyl ester 
• 98-86-2 acetophenone 
• 113416-53-8 3-Benzoyl-4-hydroxy-2-methoxy-5-oxo-1-phenyl-2,5-dihydro-1H-pyrrole-2-carboxylic acid methyl ester 
• 113416-43-6 4-benzoyl-5-methoxycarbonyl-3,5-dihydroxy-1-phenyl-2,5-dihydro-2-pyrrolone 
• 41167-58-2 2-hydroxy-4-oxo-4-phenyl-but-2-enoic acid methyl ester 
• 113416-21-0 methyl 4-oxo-4-phenyl-2-(phenylamino)but-2-enoate 
• 113416-32-3 4-benzoyl-5-methoxycarbonyl-1-phenyl-2,3-dihydropyrrole-2,3-dione 

Downstream Products

• 5071-61-4 5-phenyl-1H-pyrazole-3-carboxylic acid 
• 629609-74-1 (Z)-2-(2-oxo-2-phenylethylidene)-1,5-dihydro-4,1-benzoxazepin-3(2H)-one 
• 1391950-41-6 7,7-dimethyl-5-oxo-2-phenyl-5,6,7,8-tetrahydroquinoline-4-carboxylic acid 
• 1283714-78-2 (2Z)-2-[2-(9H-fluoren-9-ylidene)hydrazino]-4-oxo-4-phenylbut-2-enoic acid 

Relevant articles and documents

Discovery of Membrane-Bound Pyrophosphatase Inhibitors Derived from an Isoxazole Fragment

Membrane-bound pyrophosphatases (mPPases) regulate energy homeostasis in pathogenic protozoan parasites and lack human homologues, which makes them promising targets in e.g. malaria. Yet only few nonphosphorus inhibitors have been reported so far. Here, w

FIVE-MEMBERED 2,3-DIOXOHETEROCYCLES. V. SYNTHESIS OF 1-ARYL-4-AROYL-5-METHOXYCARBONYL-2,3-DIHYDRO-2,3-PYRROLEDIONES AND THEIR REACTIONS WITH WATER AND ALCOHOLS

1-Aryl-4-aroyl-5-methoxycarbonyl-2,3-dihydro-2,3-pyrrolediones were obtained from oxalyl chloride and methyl 4-aryl-2-arylamino-4-oxo-2-butenoates.They add water and alcohols reversibly with the formation of substituted 3,5-dihydroxy- and 5-alkoxy-3-hydro