96666-60-3

Basic information

• Product Name: rac-diethyl 2-(1-phenyl-3-butynyl)-malonate
• Synonyms: rac-diethyl 2-(1-phenyl-3-butynyl)-malonate
• CAS NO: 96666-60-3
• Molecular Weight: 288.343
• Mol File: 96666-60-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: rac-diethyl 2-(1-phenyl-3-butynyl)-malonate(CAS DataBase Reference)
• NIST Chemistry Reference: rac-diethyl 2-(1-phenyl-3-butynyl)-malonate(96666-60-3)
• EPA Substance Registry System: rac-diethyl 2-(1-phenyl-3-butynyl)-malonate(96666-60-3)

Safety Data

• Hazardous Substances Data: 96666-60-3(Hazardous Substances Data)

Upstream product

• 1743-36-8 1-phenylbut-3-yn-1-ol 
• 99512-36-4 Methanesulfonic acid 1-phenyl-but-3-ynyl ester 
• 105-53-3 diethyl malonate 

Downstream Products

• 96666-66-9 ethyl (2R^*,3R^*)-2-<(carbobenzyloxy)amino>-3-phenyl-5-hexynoate 
• 96666-66-9 ethyl (2R^*,3S^*)-2-<(carbobenzyloxy)amino>-3-phenyl-5-hexynoate 
• 96666-69-2 ethyl (2R^*,3R^*)-2-benzamido-3-phenyl-5-hexynoate 
• 96666-69-2 ethyl (2R^*,3S^*)-2-benzamido-3-phenyl-5-hexynoate 
• 96666-76-1 (3R^*,4R^*)-3-benzamido-4-phenyl-6(E)-(iodomethylidene)tetrahydro-2-pyranone 
• 96666-76-1 (3R^*,4S^*)-3-benzamido-4-phenyl-6(E)-(iodomethylidene)tetrahydro-2-pyranone 
• 96666-72-7 (2R^*,3R^*)-2-benzamido-3-phenyl-5-hexynoic acid 
• 96666-72-7 (2R^*,3S^*)-2-benzamido-3-phenyl-5-hexynoic acid 
• 96666-67-0 ethyl (2R^*,3R^*)-2-acetamido-3-phenyl-5-hexynoate 
• 96666-67-0 ethyl (2R^*,3S^*)-2-acetamido-3-phenyl-5-hexynoate 
• 96666-74-9 (3R^*,4R^*)-3-acetamido-4-phenyl-6(E)-(iodomethylidene)tetrahydro-2-pyranone 
• 96666-74-9 (3R^*,4S^*)-3-acetamido-4-phenyl-6(E)-(iodomethylidene)tetrahydro-2-pyranone 
• 96666-71-6 (2R^*,3R^*)-2-acetamido-3-phenyl-5-hexynoic acid 
• 96666-71-6 (2R^*,3S^*)-2-acetamido-3-phenyl-5-hexynoic acid 

Relevant articles and documents

Enol Lactone Inhibitors of Serine Proteases. The Effect of Regiochemistry on the Inactivation Behavior of Phenyl-Substituted (Halomethylene)tetra- and -dihydrofuranones and (Halomethylene)tetrahydropyranones toward α-Chymotrypsin: Stable Acyl Enzyme Inter

We have found that α-aryl-substituted halo enol lactones (I and II) are effective mechanism-based inactivators for chymotrypsin.In this study, we have investigated, for comparative purposes, halo enol lactones with aryl functions situated β and γ to the l