1161695-61-9

Basic information

• Product Name: 1-chloro-4-(4-phenylbut-1-yn-1-yl)benzene
• Synonyms: 1-chloro-4-(4-phenylbut-1-yn-1-yl)benzene
• CAS NO: 1161695-61-9
• Molecular Weight: 240.732
• Mol File: 1161695-61-9.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: 1-chloro-4-(4-phenylbut-1-yn-1-yl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: 1-chloro-4-(4-phenylbut-1-yn-1-yl)benzene(1161695-61-9)
• EPA Substance Registry System: 1-chloro-4-(4-phenylbut-1-yn-1-yl)benzene(1161695-61-9)

Safety Data

• Hazardous Substances Data: 1161695-61-9(Hazardous Substances Data)

Upstream product

• 100-44-7 benzyl chloride 
• 873-73-4 4-n-chlorophenylacetylene 
• 622-24-2 2-phenylethyl chloride 
• 103-63-9 1-phenyl-2-bromoethane 
• 106-39-8 bromochlorobenzene 
• 16520-62-0 4-Phenyl-1-butyne 
• 40277-01-8 1-(trimethylsilyl)-4-phenyl-1-butyne 
• 620-05-3 iodomethylbenzene 
• 100-51-6 benzyl alcohol 
• 637-87-6 1-Chloro-4-iodobenzene 

Downstream Products

• 1554260-32-0 (1-(4-chlorophenyl)-3,4-dihydronaphthalen-2-yl)-diphenylphosphine oxide 

Relevant articles and documents

Metal-Free Synthesis of Selenodihydronaphthalenes by Selenoxide-Mediated Electrophilic Cyclization of Alkynes

A transition-metal-free, selenium mediated electrophilic cyclization reaction was realized through a one-pot procedure between simple alkynes and triflic anhydride-activated selenoxides to give selenium containing dihydronaphthalene products. This method gave good to very high yields for all products, including selenium-substituted phenanthrene, dihydroquinoline, 2H-chromene, and coumarin, which can be further transformed to other functionalized compounds.

Visible light-driven cross-coupling reactions of alkyl halides with phenylacetylene derivatives for C(sp3)-C(sp) bond formation catalyzed by a B12 complex

Visible light-driven cross-coupling reactions of alkyl halides with phenylacetylene and its derivatives catalyzed by the cobalamin derivative (B12) with the [Ir(dtbbpy)(ppy)2]PF6 photocatalyst at room temperature are reported. The robust B12 catalyst and Ir photocatalyst provided high turnover numbers of over 33?000 for the reactions.

Formation of C(sp2) Boronate Esters by Borylative Cyclization of Alkynes Using BCl3

BCl3is an inexpensive electrophile which induces the borylative cyclization of a wide range of substituted alkynes to regioselectively form polycycles containing synthetically versatile C(sp2) boronate esters. It proceeds rapidly, with good yields and is compatible with a range of functional groups and substitution patterns. Intermolecular 1,2-carboboration of alkynes is also achieved using BCl3to generate trisubstituted vinyl boronate esters.