56147-30-9

Usage

Uses

Used in Pharmaceutical Industry:
4-n-propylpropiophenone is used as a chemical precursor for the synthesis of various pharmaceuticals. Its unique molecular structure allows it to be a key component in the production of a wide range of medications, contributing to the development of new and innovative treatments.
Used in Agrochemical Industry:
In the agrochemical industry, 4-n-propylpropiophenone is utilized as a starting material for the synthesis of various agrochemicals. Its versatility in chemical reactions enables the creation of effective products for pest control, crop protection, and other agricultural applications, thereby supporting sustainable farming practices.
Used in Chemical Research:
4-n-propylpropiophenone is also employed as a research compound in various scientific studies. Its unique properties and reactivity make it an interesting subject for exploration in the field of organic chemistry, potentially leading to new discoveries and advancements in chemical synthesis and understanding of molecular interactions.

InChI:InChI=1/C12H16O/c1-3-5-10-6-8-11(9-7-10)12(13)4-2/h6-9H,3-5H2,1-2H3

Upstream product

• 103-65-1 phenylpropane 
• 79-03-8 propionyl chloride 
• 123-62-6 propionic acid anhydride 
• 75-15-0 carbon disulfide 
• 7446-70-0 aluminium trichloride 
• 132560-67-9 α-chloro-4-propylpropiophenone 

Downstream Products

• 4815-57-0 1,4-di(n-propyl)benzene 
• 17558-64-4 1,1'-(1,4-phenylene)bis(propan-1-one) 
• 857565-87-8 1-(2,5-dipropyl-phenyl)-ethanone 
• 7709-84-4 1,4-bis-(2-bromo-propionyl)-benzene 
• 93007-14-8 1,4-Bis-(α-acetoxypropionyl)-benzol 
• 100387-99-3 C₁₂H₁₅BrO 

Relevant academic research and scientific papers

5-Aryl-imidazolin-2-ones as a scaffold for potent antioxidant and memory-improving activity

A series of 5-phenyl-substituted-N-alkyl-imidazolin-2-ones with potent radical-scavenging activity and lipid peroxidation inhibitory activity was synthesized. Many of the compounds showed memory-improving effect in animal models independent of the inhibitory activity on lipid peroxidation.

Photochemical Rearrangement of α-Chloro-Propiophenones to α-Arylpropanoic Acids: Studies on Chirality Transfer and Synthesis of (S)-(+)-Ibuprofen and (S)-(+)-Ketoprofen

A new single-step efficient photochemical approach for α-arylpropanoic acids (4) from α-chloro-propiophenones (5) is described.It involves carbonyl triplet excited state directed 1,2-aryl migration of the aryl group which has been found to be highly dependent upon the nature of the aryl substituent.The mode of the rearrangement is probed by the study of the photobehaviour of a set of optically active α-chloro-propiophenones.The results suggest that the nature of the carbonyl triplets (n, ?*/ ?, ?*) plays an important role in the chirality transfer.This method finds application in the synthesis of optically active ibuprofen (4e) and ketoprofen (26), though in moderate optical yields.