24219-37-2

Usage

Uses

Used in Organic Synthesis:
Dioctylmagnesium is used as a reagent in organic synthesis, particularly for the Grignard reaction, where it serves as a source of the nucleophilic alkyl or aryl group. This reaction is crucial for the production of various compounds.
Used in Pharmaceutical Production:
In the pharmaceutical industry, dioctylmagnesium is utilized as a reagent for the synthesis of complex organic molecules, contributing to the development of new drugs and medicines.
Used in Agrochemical Production:
Similarly, in the agrochemical sector, dioctylmagnesium is employed in the synthesis of organic compounds that are used in the creation of pesticides, herbicides, and other agricultural chemicals, enhancing crop protection and yield.
Due to its high reactivity, dioctylmagnesium must be handled with extreme caution to ensure safety during its applications in various industries.

InChI:InChI=1/2C8H17.Mg/c2*1-3-5-7-8-6-4-2;/h2*1,3-8H2,2H3;/rC16H34Mg/c1-3-5-7-9-11-13-15-17-16-14-12-10-8-6-4-2/h3-16H2,1-2H3

Upstream product

• 111-66-0 oct-1-ene 

Downstream Products

• 129126-26-7 3,5,5-Trimethyl-3-octylcyclohexanone 
• 57242-85-0 3-n-octylcyclohexanone 
• 112-05-0 nonanoic acid 
• 2216-87-7 undecan-3-one 
• 111-87-5 octanol 
• 4731-53-7 TOP 
• 693-54-9 Decan-2-one 
• 53053-78-4 methyldi(n-octyl)chlorosilane 
• 51502-63-7 methyldi(n-octyl)silane 
• 3590-84-9 tetraoctyltin 
• 6008-36-2 1-phenylnonan-1-one 
• 3429-76-3 trimethyl-octyl-silane 

Relevant academic research and scientific papers

Method for producing alkyl-bridged ligand systems and transition metal compounds

The invention relates to a method for producing highly substituted alkyl-bridged ligand systems on the basis of indene derivatives and transition metal compounds. Said alkyl-bridged ligand systems can be obtained in high yields using this method.

New Syntheses with Magnesium Hydride. Part 1: Hydromagnesiation of α-Olefins to Magnesium-dialkyls

The addition of highly active magnesium hydride to α-olefins, hydromagnesiation, is a well known reaction.The use of cheap magnesium hydride exhibiting a lower reactivity is highly desirable for industrial purposes.In a combination of chemical and mechanical activation the low reactivity of high temperature magnesium hydride could be overcome thereby making a broad variety of magnesium alkyls accessible. Key words: Magnesium alkyls; hydromagnesiation; magnesium hydride.

Diorganomagnesium Compounds from Magnesium, Hydrogen, and 1-Alkenes and Their Application in Synthesis

1-Alkenes are converted in high yields to the corresponding primary diorganomagnesium compounds by transition metal-catalyzed hydromagnesation reaction using catalytically prepared suspended (MgH2*) or dissolved magnesium hydride (MgH2').The most active hydromagnesation catalysts have been found to be combinations of zirconium tetrahalides with MgH2* or MgH2'.The reaction is highly regio- and chemoselective.The diorganomagnesium compounds prepared in situ from magnesium, hydrogen, and 1-alkenes can be applied to the synthesis of organic and organometallic compounds just as Grignard compounds (Scheme 3, reactions 3-11).Dioctylmagnesium undergoes the growth reaction with ethene in the presence of quinuclidine and is oxidized by molecular oxygen in high yield to 1-octanol. Key Words: Magnesium hydride, catalytically prepared / Hydromagnesation reactions / Magnesium, diorgano compounds, preparation from magnesium, hydrogen and 1-alkenes / Magnesium, diorgano compounds, application in syntheses / Magnesium, diorgano compounds, oxidation of

Catalytic process for producing silahydrocarbons

Silahydrocarbons such as tetraorganosilanes prepared from halo-substituted silanes and an organomagnesium compound in the presence of a catalytically effective amount of a cyanide.