62303-05-3

Basic information

• Product Name: Benzamide, 2-iodo-N-(4-methylphenyl)-
• Synonyms: 2-iodo-N-(4-tolyl)benzamide;2-iodo-N-p-tolylbenzamide;N-p-methylphenyl-2-iodobenzamide;N-p-tolyl-2-iodobenzamide;N-p-tolyl-o-iodobenzamide;N-(4-methylphenyl)-2-iodobenzamide
• CAS NO: 62303-05-3
• Molecular Formula: C14H12INO
• Molecular Weight: 337.16
• Mol File: 62303-05-3.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 339.0±35.0 °C(Predicted)
• Density: 1.631±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzamide, 2-iodo-N-(4-methylphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzamide, 2-iodo-N-(4-methylphenyl)-(62303-05-3)
• EPA Substance Registry System: Benzamide, 2-iodo-N-(4-methylphenyl)-(62303-05-3)

Safety Data

• Hazardous Substances Data: 62303-05-3(Hazardous Substances Data)

Upstream product

• 88-67-5 2-Iodobenzoic acid 
• 106-49-0 p-toluidine 
• 609-67-6 2-Iodobenzoyl chloride 

Downstream Products

• 213454-30-9 2-iodo-N-p-tolyl-benzimidoyl chloride 
• 1211900-45-6 2-(oct-1-ynyl)-N-p-tolylbenzamide 
• 1381766-63-7 2-((4-chloro-2-(dimethylamino)phenyl)ethynyl)-N-(p-tolyl)benzamide 
• 1381766-45-5 C₂₃H₁₇ClN₂O 
• 1620284-97-0 N-(p-tolyl)-2-((trifluoromethyl)thio)benzamide 
• 33238-15-2 3-phenylmethylene-2-(4-methylphenyl)isoindole-1-one 
• 871570-97-7 butyl (N-p-methylphenyl-isoindolin-1-on-3-yl)acetate 
• 582-78-5 N-(4-methylphenyl)benzamide 
• 293744-68-0 2-(2'-hydroxy-2'-methylpropynyl)-N-p-tolyl benzamide 
• 33238-15-2 (Z)-3-benzylidene-N-(4-methylphenyl)isoindolin-1-one 
• 293744-69-1 2-(2'-hydroxyethylidene)-N-p-tolyl benzamide 
• 81743-88-6 2-(4-methylphenyl)-1,2-benzisoselenazol-3(2H)-one 
• 14959-64-9 3-phenyl-2-(p-tolyl)isoquinolin-1(2H)-one 
• 2514-30-9 2-(4-tolyl)-1,2-benzisothiazol-3-one 

Relevant articles and documents

Benzisoselenazolone derivative and preparation method and application thereof

The invention provides a benzisoselenazolone derivative and a preparation method and application thereof. The compound has a structure as shown in a formula I. The invention further relates to a preparation method of the compound with the structure shown in the formula I, a pharmaceutical composition and application of the compound in preparation of anti-SARS-CoV-2Mpro drugs.

PPh3/I2/HCOOH: An efficient CO source for the synthesis of phthalimides

A straightforward and general method has been developed for the synthesis of phthalimide derivatives from 2-iodobenzamides and PPh3/I2/HCOOH in the presence of a catalytic amount of Pd(OAc)2. The reaction results demonstrate that PPh3/I2/HCOOH is a facile, efficient and safe CO source. The whole process is carried out in toluene at 80 °C and furnishes the desired products in good to excellent yields.

[N,P]-pyrrole PdCl2 complexes catalyzed the formation of dibenzo-α-pyrone and lactam analogues

We herein report the synthesis and catalytic application of a new family of [N,P] ligands based on the pyrrole ring with alpha-phosphine or phosphole units. Their palladium complexes (3a-d) were obtained in very good yields and their catalytic properties were evaluated in the direct intramolecular arylation to obtain both benzopyranones and phenanthridinones. The air stable complex 3a exhibited the best catalytic performance of this series of complexes, using 1 mol% of catalyst in combination with microwaves to promote this reaction.