998-62-9

Usage

Uses

Used in Flavor and Fragrance Industry:
Heptanal, 2-butylis used as a flavor and fragrance ingredient for its ability to impart fruity and floral scents to perfumes, cosmetics, and food items. Its pleasant and long-lasting aroma makes it a valuable addition to these products.
Used in Pharmaceutical Industry:
Although not explicitly mentioned in the provided materials, due to its potential applications, Heptanal, 2-butylcould be studied for use in the pharmaceutical industry, possibly for its scent properties in creating medication with more acceptable odors or for other medicinal purposes.
Used in Agricultural Industry:
Heptanal, 2-butylhas also been studied for its potential applications in agriculture, although the specific uses are not detailed in the provided materials. It could potentially be utilized in the development of fragrances for agricultural products or in pest control through the use of its scent properties.

Upstream product

• 124-18-5 decane 
• 201230-82-2 carbon monoxide 
• 1942-46-7 5-decyne 

Relevant academic research and scientific papers

Rhodium-catalyzed hydroformylation of alkynes employing a self-assembling ligand system

Hydroformylation of alkynes is an underdeveloped atom-economic and redox-neutral method to prepare enals. Applying a new electron poor self-assembling ligand system provides the first general rhodium-catalyst for the chemo- and stereoselective hydroformylation of dialkyl- as well as diaryl-substituted alkynes to furnish enals in excellent chemo- and stereoselectivity.

Rhodium-katalysierte Hydroformylierung innerer Alkine zu α,β-ungesaettigten Aldehyden

Keywords: Alkine; Hydroformylierungen; Katalyse; Alkene; Rhodiumverbindungen

Remarkable Effect of the Wavelength in the Photoassisted Carbonylation of the C-H Bond of Decane in the Presence of RhCl(CO)PR3)2 as the Catalyst

RhCl(CO)(Pr3)2-catalyzed and photoassisted carbonylation of decane leading to the formation of C11 aldehydes and/or 1-nonene was remarkably affected by the wavelength; irradiation with λ > 295 nm was essential to the formation of 1-nonene and undecanal.By cutting off λ 325 nm, 1-nonene formation was completely suppressed, and a series of isomeric C11 aldehydes were obtained.