CAS 925-90-6 Ethylmagnesium bromide
name | Ethylmagnesium bromide |
synonym | bromoethyl-magnesiu;ETHYLMAGNESIUM BROMIDE, CA. 3.2M SOLUTION IN 2-METHYLTETRAHYDROFURAN; |
Cas | 925-90-6 |
EINECS | 213-127-3 |
solubility | Miscible in alcohols, ketones, esters, ethers, hydrocarbons. |
Boling Point | 34.6°C |
appearance | Solution |
color | Pale yellow to brown |
purity | ≥99% |
Storage conditions | water-free area |
use | Ethylmagnesium Bromide is a useful reagent in preparation of zirconium complexes having two phenoxy-imine chelate ligands for olefin polymerization. |
Packing-Stealed and Confidential Packing,Change products Name-100% safe
Powder& Solid: The bulk powder is provided with double-layer aluminum thin bag odor-proof packaging and the small goods are replaced with plant extract animal food packaging bags
Liquid& Oil: The liquid is changed to a common product name in a sealed package, and there is a blister to prevent leakage
description
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CAS 925-90-6, also known as Ethylmagnesium bromide, is a versatile organometallic compound widely utilized in organic synthesis. Renowned for its exceptional reactivity and purity, Ethylmagnesium bromide serves as a key building block in the creation of various organic compounds, including pharmaceuticals, agrochemicals, and specialty chemicals.
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application
Grignard Reagent: Ethylmagnesium bromide is a classic example of a Grignard reagent, which is highly reactive towards a wide range of electrophiles. It serves as a key building block in organic synthesis, particularly for the formation of carbon-carbon bonds.
Carbon-Carbon Bond Formation: Ethylmagnesium bromide is utilized in the synthesis of complex organic molecules by participating in carbon-carbon bond-forming reactions. It can be employed in the preparation of alcohols, ketones, aldehydes, and other functional groups.
Functional Group Transformations: Ethylmagnesium bromide is employed in various functional group transformations, including nucleophilic substitution, addition reactions, and coupling reactions. Its reactivity allows for the conversion of functional groups, enabling the creation of diverse organic compounds.
Organometallic Chemistry: Ethylmagnesium bromide serves as a model compound for studying organometallic chemistry principles. Its reactivity with different substrates provides insights into reaction mechanisms and the behavior of organomagnesium reagents.
Pharmaceutical Synthesis: Ethylmagnesium bromide is used in the pharmaceutical industry for the synthesis of intermediates and active pharmaceutical ingredients (APIs). It enables the efficient construction of complex molecular scaffolds found in many drug molecules.
Research and Development: Ethylmagnesium bromide is a valuable tool in academic and industrial research laboratories for exploring new synthetic methodologies and developing novel compounds with potential applications in various fields.
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