17099-20-6

Upstream product

• 106-47-8 4-chloro-aniline 
• 587-04-2 m-Chlorobenzaldehyde 

Downstream Products

• 38550-05-9 2-[4-(3-chloro-styryl)-phenyl]-2H-[1,3]dioxolo[4',5':4,5]benzo[1,2-d][1,2,3]triazole 
• 59425-69-3 4,5,4',5'-tetraphenyl-2,2'-{3,3'-dichloro-4,4'-[2-(3-chloro-phenyl)-propane-1,3-diyl]-diphenyl}-bis-oxazole 
• 52823-22-0 2-[4-(3-chloro-trans-styryl)-phenyl]-5-dibenzofuran-3-yl-[1,3,4]oxadiazole 
• 59425-65-9 2,2'-{3,3'-dichloro-4,4'-[2-(3-chloro-phenyl)-propane-1,3-diyl]-diphenyl}-bis-benzooxazole 
• 76553-58-7 (4-Chloro-phenyl)-[1-(3-chloro-phenyl)-meth-(E)-ylidene]-amine; compound with trichloro-acetic acid 
• 587-04-2 m-Chlorobenzaldehyde 
• 1602-00-2 bis-(4-chloro-phenyl)-diazene 
• 102912-64-1 2-[(Z)-2-(3-Chloro-phenyl)-vinyl]-naphtho[1,2-d]thiazole 

Relevant academic research and scientific papers

Heterogeneous Catalysis with Basic Compounds to Achieve the Synthesis and C-N Cleavage of Azetidin-2-ones under Microwave Irradiation

The synthesis of azetidin-2-ones with a completely heterogeneous catalysis is reported. The use of basic compounds as solid catalysts allowed for the synthesis of azetidin-2-ones under microwave irradiation without organic additives such as triethylamine. An excellent catalyst for this transformation was Mg-Al hydroxide (MAH). The present methodology offers the advantages of non-hazardous reaction conditions, short reaction times, high yields, and catalyst reusability. Different substitution groups were tested on the imines and acyl chlorides to explore the scope of the reaction. Unconventional N-C4 bond cleavage was detected in azetidin-2-ones. MAH was characterized by N 2 adsorption-desorption, X-ray diffraction (XRD), scanning electron microscopy (SEM), and high-resolution transmission electron microscopy (HR-TEM).

Metal-free regioselective C-H amination for the synthesis of pyrazole-containing 2H-indazoles

A general and practical regioselective approach for the C-H amination of 2H-indazoles under transition-metal-free conditions was developed. A series of substrates were tested showing eminent functional group tolerance and affording the C-N functionalization products in good to excellent yields. Mechanism studies revealed that a radical process was involved in this transformation.

Polarographic investigations on azomethines: Benzal-p-chloranilines in alkaline medium and effect of substituents on half-wave potentials

Polarographic behavior of twenty-four substituted benzal-p-chloranilines has been investigated in 50percent methanol-water medium in alkaline pH range.The experimental conditions for the study were so designed that no appreciable hydrolysis of the Schiff