1430234-50-6

Basic information

• Product Name: 1-(4-chlorophenyl)-5-phenylpenta-1,4-diyn-3-one
• Synonyms: 1-(4-chlorophenyl)-5-phenylpenta-1,4-diyn-3-one
• CAS NO: 1430234-50-6
• Molecular Weight: 264.711
• Mol File: 1430234-50-6.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 1-(4-chlorophenyl)-5-phenylpenta-1,4-diyn-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(4-chlorophenyl)-5-phenylpenta-1,4-diyn-3-one(1430234-50-6)
• EPA Substance Registry System: 1-(4-chlorophenyl)-5-phenylpenta-1,4-diyn-3-one(1430234-50-6)

Safety Data

• Hazardous Substances Data: 1430234-50-6(Hazardous Substances Data)

Upstream product

• 637-44-5 phenylpropyolic acid 
• 873-73-4 4-n-chlorophenylacetylene 
• 132960-13-5 N-methoxy-N-methyl-3-phenyl-2-propynamide 

Downstream Products

• 51624-43-2 1-[4-(4-chlorophenyl)butane-1,3-diynyl]benzene 
• 1613231-72-3 1-(4-chlorophenyl)-5-phenylpenta-1,4-diyn-3-ol 

Relevant articles and documents

Enantioselective Synthesis of Bicyclopentane-Containing Alcohols via Asymmetric Transfer Hydrogenation

Compounds a containing bicyclo[1.1.1]pentane (BCP) adjacent to a chiral center can be prepared with high enantiomeric excess through asymmetric transfer hydrogenation (ATH) of adjacent ketones. In the reduction step, the BCP occupies the position distant from the η6-arene of the catalyst. The reduction was applied to the synthesis of a BCP analogue of the antihistamine drug neobenodine.