Allylmagnesium Bromide

1.0 M solution in THF, MkSeal

Reagent Code: #88894
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Alias Allyl Magnesium Bromide
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CAS Number 1730-25-2

science Other reagents with same CAS 1730-25-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.28 g/mol
Formula C₃H₅BrMg
badge Registry Numbers
MDL Number MFCD00000044
inventory_2 Storage & Handling
Density 0.851 g/mL at 25 °C
Storage room temperature

description Product Description

Allylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for introducing the allyl group into various organic molecules, enabling the formation of carbon-carbon bonds. This reagent is commonly employed in the preparation of allylic alcohols, amines, and other allyl-substituted compounds, which are important intermediates in pharmaceuticals, agrochemicals, and fine chemicals. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes it a key tool in the synthesis of complex organic structures. Additionally, it is utilized in polymerization processes to create specialized polymers with unique properties.

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Test Parameter Specification
Concentration 0.9-1.1
Appearance Grey to black liquid

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Size Availability Unit Price Quantity
inventory 100ml
10-20 days ฿6,740.00
inventory 500ml
10-20 days ฿18,960.00
inventory 800ml
10-20 days ฿26,300.00

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Allylmagnesium Bromide
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Allylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for introducing the allyl group into various organic molecules, enabling the formation of carbon-carbon bonds. This reagent is commonly employed in the preparation of allylic alcohols, amines, and other allyl-substituted compounds, which are important intermediates in pharmaceuticals, agrochemicals, and fine chemicals. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes i

Allylmagnesium bromide is widely used in organic synthesis as a Grignard reagent. It is particularly valuable for introducing the allyl group into various organic molecules, enabling the formation of carbon-carbon bonds. This reagent is commonly employed in the preparation of allylic alcohols, amines, and other allyl-substituted compounds, which are important intermediates in pharmaceuticals, agrochemicals, and fine chemicals. Its reactivity with carbonyl compounds, such as aldehydes and ketones, makes it a key tool in the synthesis of complex organic structures. Additionally, it is utilized in polymerization processes to create specialized polymers with unique properties.

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