28051-07-2

Upstream product

• 104-88-1 4-chlorobenzaldehyde 
• 3848-36-0 4-chlorobenzaldoxime 
• 62-53-3 aniline 
• 28123-63-9 4-chlorobenzohydroximoyl chloride 

Downstream Products

• 63105-01-1 4-(4-chloro-phenyl)-3-phenyl-3H-[1,2,3,5]oxathiadiazole 2-oxide 
• 1019-85-8 2-(4-chlorophenyl)benzimidazole 
• 1141-35-1 2-(4-chlorophenyl)benzoxazole 
• 53288-64-5 N-phenyl-N'-(p-chlorophenyl)carbodiimide 
• 1967-26-6 N-(4-chlorophenyl)-N'-phenylurea 

Relevant academic research and scientific papers

Iodine Promoted One-Pot Synthesis of 2-Aryl Benzoxazoles from Amidoximes via Oxidative Cyclization and Ring Contraction

A molecular I2-promoted one-pot synthesis of 2-aryl benzoxazoles has been developed by using amidoximes rather than the limited 2-aminophenols or 2-haloamides as substrates. The amidoxime substrates provided unique and efficient strategies for converting readily available aniline and benzaldehyde precursors into valuable chemicals. This transformation proceeded smoothly under transition-metal-free conditions through a sequential oxidative cyclization and ring contraction, and provided a potential route for introducing certain groups at any site of the scaffold.

Synthesis, characterization, antimicrobial activity, and QSAR studies on substituted oxadiazaboroles

This paper presents the synthesis and in vitro antimicrobial activity studies of 3,4,5-trisubstituted 4,5-dihydro-1,2,4,5-oxadiazaboroles (4) and 3,5-disubstituted 4,5-dihydro-1,2,4,5-oxadiazaboroles (7). The antimicrobial activities of the compounds were

Practical synthesis of N -substituted cyanamides via tiemann rearrangement of amidoximes

A facile and general synthesis of various N-substituted cyanamides was accomplished by the Tiemann rearrangement of amidoximes with benzenesulfonyl chlorides (TsCl or o-NsCl) and DIPEA.