7270-47-5

Upstream product

• 637-87-6 1-Chloro-4-iodobenzene 

Downstream Products

• 6922-89-0 p-chlorotriphenylmethanol 
• 730-71-2 2-chloro-1,1-bis-(4-chloro-phenyl)-2-fluoro-ethanol 
• 859946-42-2 2-bromo-4',4''-dichloro-trityl chloride 
• 845790-83-2 (4-bromo-phenyl)-bis-(4-chloro-phenyl)-methanol 
• 860587-46-8 9,10-bis-(4-chloro-phenyl)-9,10-dihydro-anthracene-9,10-diol 
• 119-56-2 (4-chlorophenyl)phenylmethanol 
• 4576-56-1 tris(p-chlorophenyl)phosphine oxide 
• 1159-54-2 tri(4-chlorophenyl)phosphine 
• 844683-40-5 (4-chlorophenyl)(4-(dimethylamino)phenyl)methanol 
• 53432-76-1 2-(4-chloro-phenyl)-2-hydroxy-1,2-diphenyl-ethanone 
• 912-17-4 1,2-diphenyl-1,2-bis-(4-chlorophenyl)-ethanediol 
• 58824-54-7 p-chlorophenylvinylcarbinol 
• 16031-54-2 1-(4-chlorophenyl)cyclopropan-1-ol 
• 113769-85-0 α-(4'-chlorophenyl)biphenyl-2-methanol 

Relevant academic research and scientific papers

An N-Fluorinated Imide for Practical Catalytic Imidations

Catalytic imidation using NFSI as the nitrogen source has become an emerging tool for oxidative carbon-nitrogen bond formation. However, the less than ideal benzenesulfonimide moiety is incorporated into products, severely detracting its synthetic value.

Efficient C(sp3)-H bond functionalization of isochroman by azadol catalysis

A novel organocatalytic C(sp3)-H bond functionalization of isochroman under practical conditions has been developed. In the presence of 5.0 mol % of AZADOL, the catalysis proceeded successfully with a broad range of substrates and nucleophiles in excellent yields.