72374-36-8

Basic information

• Product Name: Benzofuran, 2,3-dihydro-3-(phenylmethyl)-
• CAS NO: 72374-36-8
• Molecular Formula: C15H14O
• Molecular Weight: 210.276
• Mol File: 72374-36-8.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: Benzofuran, 2,3-dihydro-3-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzofuran, 2,3-dihydro-3-(phenylmethyl)-(72374-36-8)
• EPA Substance Registry System: Benzofuran, 2,3-dihydro-3-(phenylmethyl)-(72374-36-8)

Safety Data

• Hazardous Substances Data: 72374-36-8(Hazardous Substances Data)

Upstream product

• 4407-36-7 (2E)-3-phenyl-2-propen-1-ol 
• 108-95-2 phenol 
• 60333-75-7 O-allyl-2-bromophenol 
• 98-80-6 phenylboronic acid 
• 133413-61-3 1-iodo-2-[(3-phenyl-2-propen-1-yl)oxy]benzene 
• 637-87-6 1-Chloro-4-iodobenzene 
• 24892-63-5 1-allyloxy-2-iodobenzene 
• 591-50-4 iodobenzene 
• 4392-24-9 Cinnamyl bromide 
• 95-56-7 2-hydroxybromobenzene 
• 4392-24-9 3-bromo-1-phenyl-1-propenyl bromide 
• 533-58-4 2-Iodophenol 
• 120568-93-6 1-iodo-2-[(3-phenylprop-2-enyl)oxy]benzene 
• 134478-80-1 1-bromo-2-[(3-phenylprop-2-enyl)oxy]benzene 

Relevant articles and documents

Suzuki-Miyaura Csp2-Csp2Cross-Couplings Employing Nickel(II) Pincer Precatalysts: Mechanistic Investigations

This study investigates the mechanism of Suzuki-Miyaura Csp2-Csp2cross-couplings facilitated by PCP-type nickel(II) pincer complexes. By employing a combination of standard experimental and theoretical methods, it is proposed that a nickel(I)/(III) cycle is involved in this reaction and single-electron pathways likely operate in this transformation.

Copper-catalyzed cross-coupling of boronic esters with aryl iodides and application to the carboboration of alkynes and allenes

Copper-catalyzed Suzuki-Miyaura-type cross-coupling and carboboration processes are reported. The cross-couplings function well with a variety of substituted aryl iodides and aryl boronic esters and allows for orthogonal reactivity compared to palladium-catalyzed processes. The carboboration method includes both alkynes and allenes and provides access to highly substituted and stereodefined vinyl boronic esters. The alkyne carboboration method is highlighted in the simple one-pot synthesis of Tamoxifen. Cross-Cu-pling: The title cross-couplings function well with a variety of substituted aryl iodides and aryl boronic esters and allows for reactivity orthogonal to that of the palladium-catalyzed processes. The title carboboration method includes both alkynes and allenes and provides access to highly substituted and stereodefined vinyl boronic esters. The alkyne carboboration method is highlighted in a simple one-pot synthesis of Tamoxifen.

Triethylsilane-indium(III) chloride system as a radical reagent

(Chemical Equation Presented) A novel generation method of indium hydride (Cl2InH) was found by the transmetalation of InCl3 with Et3SiH. In the intramolecular cyclization of enynes, the previously reported system (NaBH4-InCl3) has a problem of side reactions with the coexistent borane. In contrast, the problem was solved by the presented system, which affords effective hydroindation of alkynes.