79837-79-9

Usage

Uses

Used in Organic Synthesis:
Phosphonium, (5-methoxy-5-oxopentyl)triphenyl-, bromide is used as a reactant in organic synthesis for the formation of carbon-carbon bonds. Its ability to facilitate these bond formations makes it a valuable component in creating complex organic molecules.
Used as a Phase-Transfer Catalyst:
In various chemical reactions, Phosphonium, (5-methoxy-5-oxopentyl)triphenyl-, bromide serves as a phase-transfer catalyst. This role is crucial in enhancing the efficiency and selectivity of reactions that involve the transfer of reactants between different phases, such as between a solid and a liquid.
Used in Medicinal Chemistry:
Due to its unique chemical properties, Phosphonium, (5-methoxy-5-oxopentyl)triphenyl-, bromide has potential applications in medicinal chemistry. It can be utilized in the development of new pharmaceutical compounds, potentially leading to advancements in drug discovery and design.
Used in Material Science:
Phosphonium, (5-methoxy-5-oxopentyl)triphenyl-, bromide also holds promise in material science. Its properties can be harnessed to create new materials with specific characteristics, contributing to the development of innovative products and technologies in various industries.

Upstream product

• 5454-83-1 5-bromovaleric acid methyl ester 
• 603-35-0 triphenylphosphine 
• 17814-85-6 (4-carboxybutyl)triphenylphosphonium bromide 
• 74-88-4 methyl iodide 

Downstream Products

• 204864-54-0 methyl-3',3-dichloro-4',4-dimethoxy-5',5-bis(methoxycarbonyl)-6,6-diphenylhexenoate 
• 155206-00-1 bimatoprost 
• 1201226-16-5 (5-(ethylamino)-5-oxopentyl)triphenylphosphonium bromide 
• 64275-76-9 (Z)-5-Undecen-1-ol 
• 51652-47-2 (Z)-dec-5-en-1-ol 
• 40642-38-4 (Z)-dodec-5-ene-1-ol 

Relevant academic research and scientific papers

Novel method for preparing Prostaglandin derivatives

Provided is a novel method for preparing prostaglandin derivatives. The method is suitable for mass production by effectively manufacturing prostaglandin derivatives with high yield. The method comprises the following steps: (S-1) adding a first reducing agent to a prostaglandin intermediate compound represented by chemical formula II and manufacturing a compound represented by chemical formula III; (S-2) manufacturing a compound represented by chemical formula IV from the compound represented by chemical formula III in the presence of a base; (S-3) adding a second reducing agent to the compound represented by chemical formula IV and manufacturing a compound represented by chemical formula V; and (S-4) performing Wittig reaction of the compound represented by chemical formula V and a compound represented by chemical formula VI, and manufacturing a compound represented by chemical formula I.COPYRIGHT KIPO 2017

Identification of very long chain unsaturated fatty acids from Ximenia oil by atmospheric pressure chemical ionization liquid chromatography-mass spectroscopy

A method is described for the enrichment of very long chain unsaturated fatty acids from total fatty acids of Ximenia oil and their identification as picolinyl esters by means of liquid chromatography-mass spectrometry with atmospheric pressure chemical ionization (LC-MS/APCI). The method is based on the use of preparative reversed phase HPLC and their subsequent identification by microbore LC-MS/APCI. The combination of these two techniques was used to identify unusual unsaturated VLCFAs up to tetracontenoic acid. All four positional isomers of tetratriacontenoic acid were also synthesized to unambiguously confirm their structure.