1010091-93-6

Basic information

• Product Name: 1-(3-(4-chlorophenyl)-1-phenylprop-2-yn-1-yl)piperidine
• Synonyms: 1-(3-(4-chlorophenyl)-1-phenylprop-2-yn-1-yl)piperidine
• CAS NO: 1010091-93-6
• Molecular Weight: 309.838
• Mol File: 1010091-93-6.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: 1-(3-(4-chlorophenyl)-1-phenylprop-2-yn-1-yl)piperidine(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(3-(4-chlorophenyl)-1-phenylprop-2-yn-1-yl)piperidine(1010091-93-6)
• EPA Substance Registry System: 1-(3-(4-chlorophenyl)-1-phenylprop-2-yn-1-yl)piperidine(1010091-93-6)

Safety Data

• Hazardous Substances Data: 1010091-93-6(Hazardous Substances Data)

Upstream product

• 873-73-4 4-n-chlorophenylacetylene 
• 100033-95-2 N-(phenylselenocarbonyl) piperidine 
• 110-89-4 piperidine 
• 78704-49-1 1-(4-chlorophenyl)-2-trimethylsilylacetylene 
• 100-52-7 benzaldehyde 

Relevant articles and documents

Magnetically recoverable Fe3O4@SBA-15: An improved catalyst for three component coupling reaction of aldehyde, amine and alkyne

We have synthesized Fe3O4 nanoparticles on mesoporous SBA-15 by an "in situ" approach. The synthesized nanocomposite material was well characterized using wide and low angle XRD, N2 adsorption-desorption isotherm, TEM, FTI

Efficient multicomponent synthesis of propargylamines catalyzed by copper nanoparticles supported on metal-organic framework derived nanoporous carbon

Cu nanoparticles were deposited on nanoporous carbon, MOF-5-C, which was fabricated by direct carbonization of MOF-5 without any additional carbon sources. The as-obtained catalyst (Cu@MOF-5-C) exhibited high catalytic activity due to the high surface area as well as hierarchical pores of MOF-5-C, and the synergetic interaction between the metal nanoparticles and support.

Expeditious and highly efficient synthesis of propargylamines using a Pd-Cu nanowires catalyst under solvent-free conditions

A heterogeneous Pd-Cu NWs-catalyzed expeditious and solvent-free synthesis of propargylamines via A3-coupling of aldehydes, alkynes, and amines has been proposed. A wide range of aldehydes, alkynes and amine substrates undergo A3-coupling to produce propargylamines in good to excellent yields with good functional tolerance, such as that towards alkoxy, hydroxy, C-X (X?=?F, Cl, Br) as well as amide and C=C bonds. Furthermore, the catalyst could be recovered easily and reused for at least 5?cycles without showing significant loss of catalytic activity.