73829-94-4

Usage

Uses

Used in Organic Synthesis:
(3-ethylpent-1-yn-1-yl)benzene is used as a building block for the synthesis of various organic compounds. Its unique structure allows for further chemical reactions and modifications, contributing to the development of new molecules with specific properties and applications.
Used in Pharmaceutical Industry:
As a precursor, (3-ethylpent-1-yn-1-yl)benzene is utilized in the production of pharmaceuticals. Its reactivity and compatibility with other chemical groups make it suitable for the synthesis of drug molecules, potentially leading to the discovery of new treatments and medications.
Used in Chemical Research:
(3-ethylpent-1-yn-1-yl)benzene serves as a subject of study in chemical research, where its properties and reactions are investigated. Understanding its behavior in different chemical environments can provide insights into the development of new synthetic methods and applications in various industries.
Used in Specialty Chemicals Production:
(3-ethylpent-1-yn-1-yl)benzene is employed as an intermediate in the production of specialty chemicals. Its versatility and reactivity enable the creation of unique chemical entities for use in specific applications, such as in materials science, coatings, or fragrances.

Upstream product

• 1809-10-5 3-bromopentane 
• 4440-01-1 lithium phenylacetylide 
• 201230-82-2 carbon monoxide 
• 52843-77-3 phenylethynyl trifluoromethyl sulfone 
• 109-66-0 pentane 
• 1483-82-5 phenylethynyl chloride 
• 73830-10-1 3-ethyl-1-phenyl-1-pentyn-3-ol 

Relevant academic research and scientific papers

Copper-catalyzed cross-coupling of alkyl and aryl grignard reagents with alkynyl halides

(Chemical Equation Presented) Good old copperl A new general procedure to couple aliphatic and aromatic Grignard reagents with alkynyl halides under copper catalysis is described (see scheme; NMP=N-methylpyrrolidinone). The reaction is chemoselective and allows preparation of a vast array of simple and functionalized internal alkynes in high yields.

Trifluoromethyl 1-radical-mediated carbonylation of alkanes leading to ethynyl ketones

The carbonylation of alkanes 1 under radical-reaction conditions was examined by using ethynyl triflone A as the unimolecular chain-transfer (UMCT) reagent. Good to moderate yields of ethynyl ketones 2 were prepared by means of this three-component coupli

SUBSTITUTION OF THE HYDROXYL GROUP IN ACETYLENIC ALCOHOLS BY HYDROGEN

Tertiary α-alkynols containing at least one phenyl group at the acetylenic carbon atom are reduced by trialkyl- and triarylsilanes in the presence of trifluoroacetic acid to the corresponding acetylene hydrocarbons.

Photoelectron Spectra of Phenylethynes, I. - Phenylethyne - Model Probe for Substituent Effects

The four low energy ?-orbitals of ethynylbenzene (1) respond differently to substitution at the alkyne site due to their respective symmetry properties.The gas phase He(I) PE spectra of the series 1 - 13 (C6H5-CC-R) are presented and the energetic tren

POLYMETALLIC DERIVATIVES OF ARYL-SUBSTITUTED ALKYNES. IX. THE PMR SPECTRA OF METALLIC DERIVATIVES WITH VARIOUS STRUCTURES IN THE SIDE CHAIN

The PMR spectra of the products from the metallation of a series of arylalkynes and arylallenes with potassium amide in liquid ammonia were investigated.It was shown that the majority of these compounds are deprotonated to form phenylpropargyl monometalli