57641-89-1

Usage

Uses

Used in the Food Industry:
5-PROPYL-1,3-CYCLOHEXANEDIONE is used as a flavoring agent for its pleasant aroma, enhancing the taste and smell of various food products.
Used in Perfumery:
In the perfume industry, 5-PROPYL-1,3-CYCLOHEXANEDIONE serves as a key ingredient in the production of perfumes and other fragrances, leveraging its agreeable scent to create desirable olfactory experiences.
Used in Organic Synthesis:
5-PROPYL-1,3-CYCLOHEXANEDIONE is utilized in organic synthesis due to its unique chemical properties, playing a role in the creation of various chemical compounds and intermediates.
Used in Pharmaceutical Research:
5-PROPYL-1,3-CYCLOHEXANEDIONE also has potential applications in pharmaceutical research, where its distinctive structure and properties may contribute to the development of new drugs and medicinal agents.
It is crucial to handle 5-PROPYL-1,3-CYCLOHEXANEDIONE with care due to its potential harmful effects if ingested or inhaled, and its ability to cause skin and eye irritation.

Upstream product

• 996-82-7 sodium diethylmalonate 
• 5609-09-6 3-hepten-2-one 
• 25290-14-6 4-Hydroxy-heptan-2-on 
• 1197155-73-9 1,5-dimethoxy-3-propylcyclohexa-1,4-diene 
• 36678-43-0 (E)-hept-4-en-2-one 

Downstream Products

• 914079-19-9 4-(3-bromo-4-hydroxy-5-nitro-phenyl)-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile 
• 914079-45-1 4-(3-bromo-4-hydroxy-phenyl)-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile 
• 57655-00-2 5-PROPYL-2-(N-p-TOLUENESULFONYLCARBAMOYL)-1,3-CYCLOHEXANEDIONE 
• 914094-67-0 4-(3-bromo-5-ethoxy-4-hydroxy-phenyl)-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carbonitrile 
• 914095-11-7 4-(3-bromo-5-ethoxy-4-hydroxy-phenyl)-2-methyl-5-oxo-7-propyl-1,4,5,6,7,8-hexahydro-quinoline-3-carboxylic acid (1S)-[1-(4-methoxy-phenyl)-ethyl]-amide 

Relevant academic research and scientific papers

Synthesis of chiloglottones - Semiochemicals from sexually deceptive orchids and their pollinators

A five-step synthesis of monoalkyl- and 2,5-dialkyl-1,3-cyclohexanediones (1) is described via a sequence involving sequential Birch reductions and alkylations from the readily accessible and inexpensive starting material, 3,5-dimethoxybenzoic acid. Two approaches were considered in which alkylation at C-2 occurs either prior or subsequent to the proposed reduction. The successful route, in which Birch reduction of a 3-alkyl resorcinol derivative (3) precedes alkylation was applied in the synthesis of chiloglottone 1 (1dc), in 58% overall yield. Chiloglottone 1 is a member of a new class of natural products, representing a known sex pheromone of the thynnine wasp Neozeleboria cryptoides and pollinator attractant in the Australian sexually deceptive orchid genus Chiloglottis. The synthetic homologues were assessed for their biological activity via electroantennographic detection.

Pyrazolopyridine cycloalkanones and process for their preparation

Novel tetrahydropyrazolo-[3,4-b]quinolinones, cyclopenta[b]pyrazolo-[4,3-e]pyridinones and cyclohepta[b]-pyrazolo[4,3-e]pyridinones, useful as anxiolytics having reduced side effects, are disclosed, including methods of preparation, pharmaceutical compositions containing them and intermediates used in their preparation.