61922-18-7

Basic information

• Product Name: ethyl 2-hydroxy-2,4-diphenyl-but-3-ynoate
• Synonyms: ethyl 2-hydroxy-2,4-diphenyl-but-3-ynoate
• CAS NO: 61922-18-7
• Molecular Weight: 280.323
• Mol File: 61922-18-7.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: ethyl 2-hydroxy-2,4-diphenyl-but-3-ynoate(CAS DataBase Reference)
• NIST Chemistry Reference: ethyl 2-hydroxy-2,4-diphenyl-but-3-ynoate(61922-18-7)
• EPA Substance Registry System: ethyl 2-hydroxy-2,4-diphenyl-but-3-ynoate(61922-18-7)

Safety Data

• Hazardous Substances Data: 61922-18-7(Hazardous Substances Data)

Upstream product

• 1603-79-8 phenylglyoxylic acid ethyl ester 
• 536-74-3 phenylacetylene 
• 4440-01-1 lithium phenylacetylide 
• 611-73-4 Benzoylformic acid 
• 64-17-5 ethanol 
• 60031-34-7 2-hydroxy-2,4-diphenylbut-3-ynoic acid 
• 1004-22-4 (phenylethynyl)sodium 

Downstream Products

• 92957-19-2 1-Methyl-4-piperidyl α-Phenyl-α-phenylethynyl-glycolate 
• 92957-18-1 1-Methyl-3-piperidyl α-Phenyl-α-phenylethynyl-glycolate 
• 126309-32-8 ethyl 2-fluoro-2,4-diphenyl-3-butynoate 
• 61922-24-5 Ethyl-2,4-diphenyl-2-hydroxi-4-oxobutanoat 
• 60031-34-7 2-hydroxy-2,4-diphenylbut-3-ynoic acid 

Relevant articles and documents

Palladium-Catalyzed Decarboxylative γ-Arylation for the Synthesis of Tetrasubstituted Chiral Allenes

An enantiospecific palladium-catalyzed decarboxylative coupling of acyclic β,γ-alkynoic acids with various aryl iodides to chiral tetrasubstituted allenes is described. The coupling reaction comprises a decarboxylative γ-palladation of α,α-disubstituted carboxylic acids to provide the tetrasubstituted allenes with complete point-to-axial chirality transfer in excellent yields.

Chemistry of novel compounds with multifunctional carbon structure. VI. Synthetic studies and 19F-nuclear magnetic resonance investigation of novel α,α-disubstituted fluoroacetates

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