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Magnesium, bis(2,2-dimethylpropyl)-, also known as magnesium diisopropylmethyl, is a chemical compound with the formula Mg(C5H11)2. It is a highly reactive metal-organic compound that serves as a powerful reducing agent in organic synthesis and as a catalyst in polymerization reactions. Due to its flammability and potential to react violently with water and air, it must be handled with extreme care. Magnesium, bis(2,2-dimethylpropyl)is also used in the production of Grignard reagents, which are essential intermediates in organic chemistry, and finds applications in the manufacturing of specialty chemicals and as a component in high-energy density batteries.

19978-31-5

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19978-31-5 Usage

Uses

Used in Organic Synthesis:
Magnesium, bis(2,2-dimethylpropyl)is used as a powerful reducing agent in organic synthesis for various chemical reactions. Its high reactivity allows it to facilitate the reduction of various functional groups, making it a valuable tool in the synthesis of complex organic molecules.
Used in Polymerization Reactions:
In the polymer industry, magnesium, bis(2,2-dimethylpropyl)is used as a catalyst to initiate and control the polymerization process. Its catalytic properties enable the formation of polymers with specific molecular weights and structures, which are essential for various applications.
Used in the Production of Grignard Reagents:
Grignard reagents, which are important intermediates in organic chemistry, are produced using magnesium, bis(2,2-dimethylpropyl)-. These reagents are versatile in their ability to undergo various reactions, such as addition, substitution, and coupling reactions, making them indispensable in the synthesis of a wide range of organic compounds.
Used in Specialty Chemicals Manufacturing:
Magnesium, bis(2,2-dimethylpropyl)is utilized in the manufacturing of specialty chemicals due to its unique properties and reactivity. Its ability to participate in various chemical reactions allows for the production of high-value specialty chemicals used in different industries.
Used in High-Energy Density Batteries:
In the energy sector, magnesium, bis(2,2-dimethylpropyl)is used as a component in high-energy density batteries. Its electrochemical properties make it suitable for use in advanced battery technologies, contributing to the development of more efficient and powerful energy storage solutions.

Check Digit Verification of cas no

The CAS Registry Mumber 19978-31-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,9,7 and 8 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 19978-31:
(7*1)+(6*9)+(5*9)+(4*7)+(3*8)+(2*3)+(1*1)=165
165 % 10 = 5
So 19978-31-5 is a valid CAS Registry Number.

19978-31-5SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name magnesium,2-methanidyl-2-methylpropane

1.2 Other means of identification

Product number -
Other names Dineopentyl-magnesium

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:19978-31-5 SDS

19978-31-5Relevant academic research and scientific papers

Reaching Milestones in the Oxygenation Chemistry of Magnesium Alkyls: towards Intimate States of O2 Activation and the First Monomeric Well-Defined Magnesium Alkylperoxide

Pietrzak, Tomasz,Justyniak, Iwona,Park, Jiwon Victoria,Terlecki, Micha?,Kapu?niak, ?ukasz,Lewiński, Janusz

, p. 2503 - 2510 (2019)

Despite decades of extensive studies on the reactivity of magnesium alkyls towards O2, the isolation and structural characterization of discrete products of these reactions still remains a challenge. Although the formation of the most frequently encountered magnesium alkoxides through unstable alkylperoxide intermediates has commonly been accepted, the latter species have been elusive for over 100 years. Probing the oxygenation of a seemingly simple well-defined neo-pentylmagnesium complex stabilized by a β-diketiminate ligand, (dippBDI)MgCH2CMe3, we report on the isolation and structure characterization of both a dimeric magnesium alkoxide [(dippBDI)Mg(μ-OCH2CMe3)]2 and the first example of monomeric magnesium alkylperoxide [(dippBDI)Mg(thf)OOCH2CMe3] (dippBDI=[(ArNCMe)2CH]? and Ar=C6H3iPr2-2,6). The formation of monomeric magnesium alkylperoxide demonstrates a crucial role of an additional Lewis base for stabilizing the most elusive oxygenation products likely due to increasing of the electron density on the metal centre. Moreover, the 1H NMR studies at ?80 °C revealed that the dissociation of a coordinated Lewis base from the solvated complex (dippBDI)Mg(L)CH2CMe3 (where L=thf or 4-methylpyridine) is likely not required prior to the effective attack of an O2 molecule on the metal centre and the four-coordinate alkylmagnesium complex reacts smoothly with O2 under these conditions. The results can be expected to aid future engineering of various organomagnesium/O2-based reaction systems.

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