202207-02-1

Basic information

• Product Name: 2-chloro-N-(2-iodophenyl)benzamide
• Synonyms: 2-chloro-N-(2-iodophenyl)benzamide
• CAS NO: 202207-02-1
• Molecular Weight: 357.578
• Mol File: 202207-02-1.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: 2-chloro-N-(2-iodophenyl)benzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 2-chloro-N-(2-iodophenyl)benzamide(202207-02-1)
• EPA Substance Registry System: 2-chloro-N-(2-iodophenyl)benzamide(202207-02-1)

Safety Data

• Hazardous Substances Data: 202207-02-1(Hazardous Substances Data)

Upstream product

• 615-43-0 2-iodophenylamine 
• 609-65-4 o-chlorobenzoyl chloride 

Downstream Products

• 1039984-47-8 2-hydroxy-N-(2-iodophenyl)benzamide 
• 6269-46-1 2-(2-chlorophenyl)-1,3-benzothiazole 
• 4765-51-9 2-(2-chlorophenyl)benzo[d]1,3-oxazin-4-one 
• 3164-09-8 2-(2-chlorophenyl)-1,3-benzoxazole 

Relevant articles and documents

Hydroarylation of Arenes via Reductive Radical-Polar Crossover

A photocatalytic system for the dearomative hydroarylation of benzene derivatives has been developed. Using a combination of an organic photoredox catalyst and an amine reductant, this process operates through a reductive radical-polar crossover mechanism where aryl halide reduction triggers a regioselective radical cyclization event, followed by anion formation and quenching to produce a range of complex spirocyclic cyclohexadienes. This light-driven protocol functions at room temperature in a green solvent system (aq. MeCN) without the need for precious metal-based catalysts or reagents or the generation of stoichiometric metal byproducts.