65248-53-5

Usage

Uses

Used in Pharmaceutical Industry:
(4-chlorobenzyl) isopropyl ketone is used as an intermediate for the synthesis of various pharmaceuticals. Its presence allows for the introduction of the chlorine atom into different organic molecules, which can be crucial for the development of new drugs with specific therapeutic properties.
Used in Fragrance Industry:
In the fragrance industry, (4-chlorobenzyl) isopropyl ketone is utilized as a key component in the creation of various scents. Its unique chemical structure contributes to the development of novel fragrances with distinct olfactory profiles.
Used in Chemical Industry:
(4-chlorobenzyl) isopropyl ketone also serves as a reagent in organic chemistry reactions. Its ability to introduce the chlorine atom into organic molecules makes it a valuable tool for researchers and chemists working on the synthesis of new compounds with potential applications in various fields.
Overall, (4-chlorobenzyl) isopropyl ketone is a versatile compound with applications in the pharmaceutical, fragrance, and chemical industries, thanks to its unique chemical properties and the potential for synthesizing complex organic molecules.

Upstream product

• 78-82-0 Isobutyronitrile 
• 104-83-6 1-Chloro-4-(chloromethyl)benzene 
• 66633-08-7 4-(4-chloro-benzyl)-4-isopropyl-2-phenyl-4H-oxazol-5-one 
• 79-30-1 isobutyryl chloride 
• 66633-11-2 2-Benzoylamino-2-(4-chloro-benzyl)-3-methyl-butyric acid 

Downstream Products

• 14276-94-9 (3-methylbutyl)-4-chlorobenzene 
• 152297-00-2 1-dimethylamino-2-(4-chlorophenyl)-4-methyl-pent-1-en-3-one 
• 96223-56-2 1-[(4R,5S)-4-(4-Chloro-phenyl)-5-isopropyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 96223-56-2 1-[(4R,5R)-4-(4-Chloro-phenyl)-5-isopropyl-2-oxo-2λ⁴-[1,3,2]dioxathiolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 107659-83-6 (4R,5S)-4-(4-Chloro-phenyl)-5-isopropyl-4-[1,2,4]triazol-1-ylmethyl-[1,3]dioxolan-2-one 
• 107659-84-7 (4R,5R)-4-(4-Chloro-phenyl)-5-isopropyl-4-[1,2,4]triazol-1-ylmethyl-[1,3]dioxolan-2-one 
• 94147-79-2 2-(4-Chloro-phenyl)-2-hydroxy-4-methyl-1-[1,2,4]triazol-1-yl-pentan-3-one 
• 107679-89-0 1-[(4R,5S)-4-(4-Chloro-phenyl)-5-isopropyl-[1,3]dioxolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 96223-62-0 1-[(4R,5R)-4-(4-Chloro-phenyl)-5-isopropyl-[1,3]dioxolan-4-ylmethyl]-1H-[1,2,4]triazole 
• 107659-57-4 (2S,3S)-2-(4-Chloro-phenyl)-4-methyl-1-[1,2,4]triazol-1-yl-pentane-2,3-diol 
• 107659-56-3 (2S,3R)-2-(4-Chloro-phenyl)-4-methyl-1-[1,2,4]triazol-1-yl-pentane-2,3-diol 
• 107659-19-8 2-(4-Chloro-phenyl)-2-hydroxy-1-imidazol-1-yl-4-methyl-pentan-3-one 

Relevant academic research and scientific papers

A Nucleophilic Strategy for Enantioselective Intermolecular α-Amination: Access to Enantioenriched α-Arylamino Ketones

The enantioselective addition of anilines to azoalkenes was accomplished through the use of a chiral phosphoric acid catalyst. The resulting α-arylamino hydrazones were obtained in good yields and excellent enantioselectivities and provide access to enantioenriched α-arylamino ketones. A serendipitous kinetic resolution of racemic α-arylamino hydrazones is also described.