62059-61-4

Basic information

• Product Name: 1-phenyloct-1-yn-3-one
• Synonyms: 1-Octyn-3-one, 1-phenyl-
• CAS NO: 62059-61-4
• Molecular Formula: C₁₄H₁₆O
• Molecular Weight: 200.2762
• Mol File: 62059-61-4.mol
• Article Data: 11

Chemical Properties

• Boiling Point: 317.2°C at 760 mmHg
• Flash Point: 118.8°C
• Density: 0.99g/cm³
• Vapor Pressure: 0.000391mmHg at 25°C
• Refractive Index: 1.525
• CAS DataBase Reference: 1-phenyloct-1-yn-3-one(CAS DataBase Reference)
• NIST Chemistry Reference: 1-phenyloct-1-yn-3-one(62059-61-4)
• EPA Substance Registry System: 1-phenyloct-1-yn-3-one(62059-61-4)

Safety Data

• Hazardous Substances Data: 62059-61-4(Hazardous Substances Data)

Usage

Physical state

Yellowish liquid

Odor

Slightly floral

Common uses

Building block in the synthesis of pharmaceuticals and other organic compounds

Versatility

Versatile intermediate in organic chemistry

Production

Used in the production of various specialty chemicals

Research and development

Starting material for the synthesis of complex organic molecules

Biological and pharmacological activities

Potential activities have been studied

Upstream product

• 51499-41-3 hexanoic acid bromide 
• 1004-22-4 (phenylethynyl)sodium 
• 2051-49-2 n-hexanoic anhydride 
• 1119-67-1 1-iodo-1-hexyne 
• 4440-01-1 lithium phenylacetylide 
• 27975-79-7 1-phenyloct-1-yn-3-ol 
• 16967-02-5 1-phenyl-1-octyne 
• 1006722-47-9 C₁₁H₂₀O₃ 
• 536-74-3 phenylacetylene 
• 142-61-0 Hexanoyl chloride 
• 21890-32-4 tetrakis(phenylethynyl)tin 
• 66-25-1 hexanal 
• 2170-06-1 1-Phenyl-2-(trimethylsilyl)acetylene 
• 123-66-0 Ethyl hexanoate 

Downstream Products

• 14633-16-0 3-pentyl-5-phenylisoxazole 
• 108161-55-3 (E)-1-Iodo-1-phenyl-oct-1-en-3-one 
• 108161-54-2 (1Z)-1-iodo-1-phenyl-1-octen-3-one 
• 56438-78-9 (Z)-1-Phenyloct-1-en-3-on 
• 29478-39-5 (E)-1-phenyloct-1-en-3-one 
• 1028440-28-9 1-(5-phenyl-1H-[1,2,3]triazol-4-yl)hexan-1-one 
• 22089-86-7 Phenyl-1,2-heptanedione 

Relevant articles and documents

Bifunctional Borane Catalysis of a Hydride Transfer/Enantioselective [2+2] Cycloaddition Cascade

Herein, we present a mild and efficient method for synthesizing enantioenriched tetrahydroquinoline-fused cyclobutenes through a cascade reaction between 1,2-dihydroquinolines and alkynones with catalysis by chiral spiro-bicyclic bisboranes. The bisborane

Alkynylation of Csp2 (O)–H Bonds Enabled by Photoredox-Mediated Hydrogen-Atom Transfer

The development of new hydrogen-atom transfer (HAT) strategies within the framework of photoredox catalysis is highly appealing for its power to activate a desired C?H bond in the substrate leading to its selective functionalization. Reported here is the first photoredox-mediated hydrogen-atom transfer method for the efficient synthesis of ynones, ynamides, and ynoates with high regio- and chemoselectivity by direct functionalization of Csp2 (O)?H bonds. The broad synthetic application of this method has been demonstrated by the selective functionalization of C(O)?H bonds within complex molecular scaffolds.

Solvent free synthesis of ynones using magnetically recoverable Copper-ferrite nanoparticles

A general and efficient biogenic CuFe2O4 MNP's catalyzed synthesis of ynones has been reported for the first time. The reaction occurs in solvent free conditions without the use of any harsh conditions. The average diameter of the na