104682-98-6

Basic information

• Product Name: N-(2-(2-phenylethynyl)phenyl)benzamide
• Synonyms: N-(2-(2-phenylethynyl)phenyl)benzamide
• CAS NO: 104682-98-6
• Molecular Weight: 297.356
• Mol File: 104682-98-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: N-(2-(2-phenylethynyl)phenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-(2-phenylethynyl)phenyl)benzamide(104682-98-6)
• EPA Substance Registry System: N-(2-(2-phenylethynyl)phenyl)benzamide(104682-98-6)

Safety Data

• Hazardous Substances Data: 104682-98-6(Hazardous Substances Data)

Upstream product

• 13141-38-3 2-phenylethynylaniline 
• 98-88-4 benzoyl chloride 
• 536-74-3 phenylacetylene 
• 1516899-07-2 N,N-dibenzyl-2-(phenylethynyl)aniline 
• 35010-17-4 1-nitro-2-phenylethynyl-benzene 
• 93-97-0 benzoic acid anhydride 
• 15310-02-8 o-iodobenzanilide 
• 615-43-0 2-iodophenylamine 
• 13146-23-1 copper(I) phenylacetylenide 
• 101010-05-3 C₁₇H₁₀F₆NO₅Tl 

Downstream Products

• 1267460-80-9 (Z)-4-benzylidene-2-phenyl-4H-benzo[d][1,3]oxazine 
• 1415218-85-7 N-[2-(2-oxo-2-phenylacetyl)phenyl]benzamide 
• 1456546-94-3 4-(iodo(phenyl)methylene)-2-phenyl-4H-benzo[d][1,3]oxazine 
• 26862-65-7 phenyl (2-phenyl-1H-indol-3-yl)methanone 
• 99872-44-3 phenyl(3-phenyl-1H-indol-1-yl)methanone 
• 1612876-04-6 C₂₇H₂₀N₂Se 
• 1612876-10-4 (Z)-2-phenyl-4-(phenyl(phenylselanyl)methylene)-4H-benzo[d][1,3]oxazine 

Relevant articles and documents

Regioselective Synthesis of 2° Amides Using Visible-Light-Induced Photoredox-Catalyzed Nonaqueous Oxidative C-N Cleavage of N, N-Dibenzylanilines

A visible-light-driven photoredox-catalyzed nonaqueous oxidative C-N cleavage of N,N-dibenzylanilines to 2° amides is reported. Further, we have applied this protocol on 2-(dibenzylamino)benzamide to afford quinazolinones with (NH4)2S2O8 as an additive. Mechanistic studies imply that the reaction might undergo in situ generation of α-amino radical to imine by C-N bond cleavage followed by the addition of superoxide ion to form amides.

Iron(III) chloride/diorganyl diselenides promoted regio-and stereoselective cyclization of ortho-alkynylanilides: Synthesis of (Z)-4-(chalcogen) methylenebenzoxazines

Intramolecular 6-exo-dig cyclization of ortho-alkynylanilides has been employed in a regioand stereoselective synthesis of (Z)-4-(chalcogen)- methylenebenzoxazines. Several reaction parameters were screened for the efficient cyclization of orthoalkynylani

Silver-catalyzed cascade cyclization-stannylation of o-alkynylaniline derivatives with 2-tributylstannylfuran: An efficient synthesis of (3-indolyl)stannanes

A straightforward synthesis of (3-indolyl)stannanes through silver-catalyzed cyclization-stannylation of N-electron-withdrawing group-substituted o-alkynylanilines in the presence of 2-tributylstannylfuran is developed. This method offers several advantages such as no requirement of additional ligands, high efficiency and a wide reaction scope.