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Ethylmagnesium Bromide CAS 925-90-6

CAS NO. 925-90-6
Molecular formula: C2H5BrMg

Ethylmagnesium Bromide (also known as EtMgBr) is a chemical compound that belongs to the Grignard Reagents or organomagnesium compounds class. Grignard compounds are highly reactive organic metals composed of a magnesium-bonded alkyl, or aryl, group (in this case an ethyl), and a halogen, in this instance bromine. The chemical formula of ethylmagnesium is C2H5MgBr.

SKU: JH-925-90-6 Category: Tag:

Description

Ethylmagnesium Bromide, also known as EtMgBr, CAS 925-90-6,  is an indispensable and powerful reagent for organic chemistry. It allows the synthesis and preparation of many pharmaceuticals, specialty chemicals, and agrochemicals. Its versatility and reactivity make it an essential part of modern organic synthesis.

Ethylmagnesium Bromide EtMgBr CAS 925-90-6

Name

Ethylmagnesium bromide

Cas No.

925-90-6

Formula

C2H5BrMg

Synonyms

Bromoethylmagnesium
Ethvlmagnesiumbromide
Ethylmagnesium bromide
Magnesium, bromoethyl-
Ethyl magnesium bromide

Molecular weight

133.27

Appearance

Pale yellow to brown solution

Density

1.02 g/mL at 25 °C

Melting Point

-116.3°C

Boiling Point

34.6°C

Flashing Point

<−30 °F

Water Soluble

Reacts with water.

Stability

Flammable, dangerous fire risk.

Usage

Ethylmagnesium Bromide is a useful reagent in preparation of zirconium complexes having two phenoxy-imine chelate ligands for olefin polymerization.

 

Markets/Application:

Reactivity: Ethylmagnesium Bromide is highly reactive due to the magnesium-carbon bonds. It reacts readily with various organic molecules, including ketones, esters, aldehydes and other electrophilic substances. Its reactivity makes this reagent a valuable tool in organic synthesis.

Synthetic Applications: EtMgBr is used widely in organic synthesis, as a nucleophilic agent. It is used to introduce an ethyl ring into a molecule. This can be useful in building complex organic molecules. The Grignard Reagents are essential tools for organic chemistry to create carbon-carbon bonds.

Preparation: Ethylmagnesium Bromide EtMgBr is usually prepared by reacting Diethyl Ether (Et2O), magnesium metal (Mg), and ethyl chloride (C2H5Br), in a controlled atmosphere, often in anhydrous conditions (without water).

Safety precautions: Ethylmagnesium Bromide EtMgBr can catch fire spontaneously when exposed to the air. It is highly reactive, pyrophoric and volatile. It must be handled carefully due to its potential hazards and reactivity. This is usually done in an inert, dry atmosphere such as in a glove box or under nitrogen or argon gas. When working with this substance, it is essential to take the necessary safety precautions, such as wearing protective gear.

Applications: Ethylmagnesium Bromide EtMgBr can be used for a variety of chemical reactions. These include nucleophilic additions of carbonyl compounds to form carbon-carbon bonds and in various transformations of organic synthesis. It is a versatile and useful reagent in both the chemical and laboratory industries.

 

Synonyms:

EtMgBr

Bromoethylmagnesium

Ethvlmagnesiumbromide

Ethylmagnesium bromide

Magnesium, bromoethyl-

Ethyl magnesium bromide

 

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