15310-02-8

Basic information

• Product Name: N-(2-iodophenyl)benzamide
• CAS NO: 15310-02-8
• Molecular Formula: C₁₃H₁₀INO
• Molecular Weight: 323.1291
• Mol File: 15310-02-8.mol
• Article Data: 27

Chemical Properties

• Boiling Point: 308°C at 760 mmHg
• Flash Point: 140.1°C
• Density: 1.697g/cm³
• Vapor Pressure: 0.0007mmHg at 25°C
• Refractive Index: 1.701
• CAS DataBase Reference: N-(2-iodophenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(2-iodophenyl)benzamide(15310-02-8)
• EPA Substance Registry System: N-(2-iodophenyl)benzamide(15310-02-8)

Safety Data

• Hazardous Substances Data: 15310-02-8(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 98-88-4 benzoyl chloride 
• 591-50-4 iodobenzene 
• 201230-82-2 carbon monoxide 
• 451-40-1 phenyl benzyl ketone 
• 611-73-4 Benzoylformic acid 
• 613-90-1 benzoyl cyanide 
• 346689-44-9 4-chloro-N-(2-iodophenyl)benzamide 
• 65-85-0 benzoic acid 

Downstream Products

• 93-98-1 N-phenyl benzoyl amide 
• 1015-89-0 6(5H)-phenanthridinone 
• 26625-17-2 1,1′-biphenyl-2,2′-diamine dibenzamide 
• 85445-09-6 N-(2-iodophenyl)benzothioamide 
• 138883-34-8 N-(2-iodophenyl)-N-methylbenzamide 
• 339267-25-3 2-(2-Iodophenyl)-N-methoxymethylbenzamide 
• 848171-87-9 N-(but-3-en-1-yl)-N-(2-iodophenyl)benzamide 
• 848171-99-3 N-(2-iodophenyl)-N-(pent-4-en-1-yl)benzamide 
• 848171-88-0 N-hex-5-en-1-yl-N-(2-iodophenyl)benzamide 
• 833-50-1 2-phenylbenzo[d]oxazole 
• 175846-71-6 N-(2-vinyl-phenyl)benzamide 
• 54147-92-1 N-(4'-methoxy-biphenyl-2-yl)-benzamide 
• 93013-26-4 1-allyl-2-phenyl-1H-benzo[d]imidazole 
• 883-93-2 2-Phenylbenzothiazole 

Relevant articles and documents

Aniline-Type Hypervalent Iodine(III) for Intramolecular Cyclization via C?H Bond Abstraction of Hydrocarbons Containing N- and O-Nucleophiles

We developed a method for the preparation of (diacetoxyiodo)-2-(N-alkylamido)benzene as an aniline-type hypervalent iodine(III). We also achieved direct cyclizations via C?H bond abstraction, such as the Hofmann-L?ffler-Freytag reaction, a direct amination, and a direct lactonization, using the aniline-type hypervalent iodine(III) to obtain corresponding products in high yields. (Figure presented.).

Novel and efficient heterogeneous polymer supported copper catalyst for synthesis of 2-substituted Benzoxazoles from 2-Haloanilides

A novel polymer supported copper complex is prepared by the immobilization of copper iodide on chemically modified polyacrylonitrile and its application in heterogeneous catalysis is described. The catalyst was prepared by easy method via synthetic modification of Polyacrylonitrile (PAN) using ethylene diamine followed by the complexation with CuI. After characterization, this complex was explored as a green and efficient heterogeneous catalyst for the synthesis of 2-benzoxazoles from 2-haloanilides. The reaction was performed without adding additional ligand and the catalyst shows activity over a broad range of substrates with quantitative product yields. The catalyst was easily recovered by simple filtration and reused successfully for further cycle.

Synthesis of Aminated Phenanthridinones via Palladium/Norbornene Catalysis

An ortho-amination, ipso-C-H arylation mediated by palladium/norbornene cooperative catalysis is reported. This reaction proceeds through a sequential intermolecular C-N bond formation process followed by intramolecular C-H activation of a tethered arene. The products, aminated phenanthridinones, were generated in moderate to good yields. This method is also applicable to the formation of dibenzazepinones.