91368-25-1

Basic information

• Product Name: 6-phenylhex-3-en-5-yne-2-one
• Synonyms: 6-phenylhex-3-en-5-yne-2-one
• CAS NO: 91368-25-1
• Molecular Weight: 170.211
• Mol File: 91368-25-1.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: 6-phenylhex-3-en-5-yne-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenylhex-3-en-5-yne-2-one(91368-25-1)
• EPA Substance Registry System: 6-phenylhex-3-en-5-yne-2-one(91368-25-1)

Safety Data

• Hazardous Substances Data: 91368-25-1(Hazardous Substances Data)

Upstream product

• 6738-06-3 phenylethynylmagnesium bromide 
• 1809-59-2 1-diethylamino-1-buten-3-one 
• 2579-22-8 Phenylpropargyl aldehyde 
• 21204-67-1 methyl (triphenylphosphoranylidene)acetate 
• 67-64-1 acetone 
• 1439-36-7 1-triphenylphosphoranylidene-2-propanone 
• 53133-27-0 4-(N-methyl-anilino)-but-3-en-2-one 

Downstream Products

• 14171-89-2 1-phenyl-5-hexanone 

Relevant articles and documents

Chemo- and Regioselective Synthesis of Alkynyl Cyclobutanes by Visible Light Photocatalysis

Here is the first visible light catalytic intermolecular cross [2 + 2] cycloaddition of enynes with alkenes to alkynyl cyclobutanes established with good functional group tolerance and high reaction efficiency and selectivity. Detailed studies reveal that

Activation of Chiral (Salen)AlCl Complex by Phosphorane for Highly Enantioselective Cyanosilylation of Ketones and Enones

Phosphoranes 2 are identified as a class of effective Lewis bases to activate chiral (salen)AlCl complex 1 to enhance its electrophilicity. Accordingly, a three-component catalyst system consisting of complex 1, phosphorane 2e, and Ph3PO is developed as a powerful tool for asymmetric ketone cyanosilylation. In particular, an unprecedented highly enantioselective cyanosilylation of linear aliphatic ketones is achieved. A tandem Wittig-cyanosilylation sequence starting from phosphorane 2a and enals 10 is further achieved, which internally utilizes the Ph3PO byproduct and remaining phosphorane 2a as cocatalysts for cyanosilylation of α,β,γ,δ-unsaturated enones, providing atom-efficient access to valuable chiral conjugated dienes and enynes. The high efficiency of the cyanosilylation originates from orthogonal activation of both (salen)AlCl complex 1 and cyanotrimethylsilane by the phosphorane and Ph3PO, respectively. This mechanistic insight is supported by NMR, MS, and ReactIR analyses and DFT calculations. Furthermore, the formation of charged complexes through the activation of chiral complex 1 by phosphorane 2a is confirmed by electrical conductivity experiments.