7501-56-6

Usage

Uses

Used in Organic Synthesis:
(3-chloro-4-nitrophenyl)(phenyl)methanone is used as an intermediate in organic synthesis for the production of various chemical compounds. Its unique structure and reactivity make it a valuable building block in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Research:
(3-chloro-4-nitrophenyl)(phenyl)methanone is used as a research compound in pharmaceutical research for the development of new drugs. Its chemical properties can be exploited to design and synthesize novel drug candidates with potential therapeutic applications.
Used in Chemical Industry:
(3-chloro-4-nitrophenyl)(phenyl)methanone is used as a specialty chemical in the chemical industry for various applications, such as the production of dyes, pigments, and other organic compounds.
It is important to handle (3-chloro-4-nitrophenyl)(phenyl)methanone with caution, as it may pose health and environmental hazards if not managed properly.

Upstream product

• 55737-29-6 3-chloro-4-nitro-benzoic acid chloride 
• 71-43-2 benzene 
• 143064-49-7 1-(Ethoxy-phenyl-methyl)-1H-benzotriazole 
• 88-73-3 2-Chloronitrobenzene 
• 39608-47-4 3-chloro-4-nitrobenzoic acid 

Downstream Products

• 64133-91-1 (7-chloro-3-phenyl-benzo[c]isoxazol-5-yl)-phenyl-methanone 
• 39055-81-7 5-Benzoyl-3-chloro-2-hydroxy-benzonitrile 
• 64133-85-3 2-(4-Benzoyl-2-chloro-phenyl)-2-phenyl-butyronitrile 
• 64133-86-4 2-(4-Benzoyl-2-chloro-phenyl)-2,3-diphenyl-propionitrile 
• 64133-84-2 2-(4-benzoyl-2-chlorophenyl)-2-phenylpropanenitrile 
• 637331-77-2 3-(methylamino)-4-nitrobenzophenone 
• 637331-78-3 4-amino-3-(methylamino)benzophenone 
• 64133-92-2 2-Chlor-4.6-dibenzoylanilin 
• 72106-42-4 5-benzoyl-2-nitrobenzonitrile 
• 84437-63-8 2-chloro-4-benzylnitrobenzene 
• 252019-50-4 2-Chloro-4-benzylaniline 
• 159390-17-7 4-amino-3-cyanobenzophenone 

Relevant academic research and scientific papers

Synthesis and antiparasitic activity of Albendazole and Mebendazole analogues

Albendazole (Abz) and Mebendazole (Mbz) analogues have been synthesized and in vitro tested against the protozoa Giardia lamblia, Trichomonas vaginalis and the helminths Trichinella spiralis and Caenorhabditis elegans. Results indicate that compounds 4a, 4b (Abz analogues), 12b and 20 (Mbz analogues) are as active as antiprotozoal agents as Metronidazole against G. lamblia. Compound 9 was 58 times more active than Abz against T. vaginalis. Compounds 8 and 4a also shown high activity against this protozoan. Compounds 4b and 5a were as active as Abz. None of the Mbz analogues showed activity against T. vaginalis. The anthelmintic activity presented by these compounds was poor.

Reactions of 1-(benzotriazol-1-yl)-1-phenoxyalkane and (benzotriazol-1- yl)ethoxyphenylmethane anions with nitroarenes: A new approach to alkyl and aryl p-nitroaryl ketones

p-Nitroaryl alkyl ketones and p-nitroaryl aryl ketones are prepared regioselectively by reactions of non-functionalized nitroarenes and benzotriazole stabilized carbanions.