152858-50-9

Basic information

• Product Name: 6-phenyl-5-hexyne-1-nitrile
• Synonyms: 6-phenyl-5-hexyne-1-nitrile
• CAS NO: 152858-50-9
• Molecular Weight: 169.226
• Mol File: 152858-50-9.mol
• Article Data: 18

Chemical Properties

• CAS DataBase Reference: 6-phenyl-5-hexyne-1-nitrile(CAS DataBase Reference)
• NIST Chemistry Reference: 6-phenyl-5-hexyne-1-nitrile(152858-50-9)
• EPA Substance Registry System: 6-phenyl-5-hexyne-1-nitrile(152858-50-9)

Safety Data

• Hazardous Substances Data: 152858-50-9(Hazardous Substances Data)

Upstream product

• 536-74-3 phenylacetylene 
• 14918-21-9 5-hexynonitrile 
• 945-51-7 1,1'-sulfinylbisbenzene 
• 501-65-5 diphenyl acetylene 
• 591-50-4 iodobenzene 
• 7714-33-2 methyl phenylethynyl sulfide 
• 5332-06-9 4-bromobutanenitrile 

Downstream Products

• 1454697-26-7 5,8-dimethyl-9-phenyl-2,3-dihydro-1H-cyclopenta[b]quinoline 
• 1454697-24-5 5-fluoro-9-phenyl-2,3-dihydro-1H-cyclopenta[b]quinoline 
• 1454697-22-3 9-phenyl-7-(trifluoromethyl)-2,3-dihydro-1H-cyclopenta[b]quinoline 
• 1454697-20-1 7-methyl-9-phenyl-2,3-dihydro-1H-cyclopenta[b]quinoline 
• 10265-82-4 9-phenyl-2,3-dihydro-1H-cyclopenta[b]quinoline 
• 1186623-44-8 C₂₂H₂₁NO₂ 
• 690660-82-3 (E)-6-oxo-6-phenylhex-4-enenitrile 
• 16424-52-5 (E)-6-Phenylhex-5-enenitrile 

Relevant articles and documents

Thieme Chemistry Journal awardees - Where are they now? Synthesis of diamantane-derived N-heterocyclic carbenes and applications in catalysis

Novel diamantyl-substituted imidazolium salts have been synthesized, characterized and, in addition, analyzed by single-crystal structural analysis. The corresponding NHCs (a-IDAd and m-IDAd) have been prepared in solution and have been characterized by N

The First Applications of Carbene Ligands in Cross-Couplings of Alkyl Electrophiles: Sonogashira Reactions of Unactivated Alkyl Bromides and Iodides

A Pd/N-heterocyclic carbene-based catalyst achieves the Sonogashira coupling of an array of functionalized, β-hydrogen-containing alkyl bromides and iodides under mild conditions. By furnishing the first example of a nonphosphine-based palladium catalyst

Copper-catalysed Csp3-Csp cross-couplings between cyclobutanone oxime esters and terminal alkynes induced by visible light

A novel transformation for the construction of Csp3-Csp bonds was achieved via a photo-induced copper-catalysed C-C bond cleavage. This approach was applied to prepare a series of highly functionalized alkynyl nitriles using readily available cyclobutanones and terminal alkynes. Mechanistic exploration showed that the in situ generated copper acetylide complex is an effective photosensitive catalyst to promote the C-C bond cleavage of cycloketoxime esters through a radical process.

Fine-tuned organic photoredox catalysts for fragmentation-alkynylation cascades of cyclic oxime ethers

Fine-tuned organic photoredox catalysts are introduced for the metal-free alkynylation of alkylnitrile radicals generated via oxidative ring opening of cyclic alkylketone oxime ethers. The redox properties of the dyes were determined by both cyclic voltam