2-(1,3-Dioxolan-2-yl)]ethyl]zinc bromide solution

0.5 M in THF

Reagent Code: #77830
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CAS Number 307531-83-5

science Other reagents with same CAS 307531-83-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.42 g/mol
Formula C₅H₉BrO₂Zn
badge Registry Numbers
MDL Number MFCD02260129
thermostat Physical Properties
Boiling Point 65℃
inventory_2 Storage & Handling
Density 0.984 g/mL at 25℃
Storage 2-8℃

description Product Description

This chemical is primarily used in organic synthesis as a reagent for introducing the 2-(1,3-dioxolan-2-yl)ethyl group into various organic molecules. It is particularly valuable in the formation of carbon-carbon bonds, making it useful in the synthesis of complex organic compounds. The dioxolane group in the reagent can act as a protecting group for carbonyl compounds, allowing selective reactions to occur at other sites within the molecule. This reagent is often employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over molecular structure is critical. Its application in organozinc chemistry also makes it a key component in cross-coupling reactions, such as Negishi coupling, which is widely used in the construction of carbon frameworks in organic chemistry.

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inventory 50ml
10-20 days ฿26,532.00

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2-(1,3-Dioxolan-2-yl)]ethyl]zinc bromide solution
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This chemical is primarily used in organic synthesis as a reagent for introducing the 2-(1,3-dioxolan-2-yl)ethyl group into various organic molecules. It is particularly valuable in the formation of carbon-carbon bonds, making it useful in the synthesis of complex organic compounds. The dioxolane group in the reagent can act as a protecting group for carbonyl compounds, allowing selective reactions to occur at other sites within the molecule. This reagent is often employed in the preparation of pharmaceu

This chemical is primarily used in organic synthesis as a reagent for introducing the 2-(1,3-dioxolan-2-yl)ethyl group into various organic molecules. It is particularly valuable in the formation of carbon-carbon bonds, making it useful in the synthesis of complex organic compounds. The dioxolane group in the reagent can act as a protecting group for carbonyl compounds, allowing selective reactions to occur at other sites within the molecule. This reagent is often employed in the preparation of pharmaceuticals, agrochemicals, and fine chemicals, where precise control over molecular structure is critical. Its application in organozinc chemistry also makes it a key component in cross-coupling reactions, such as Negishi coupling, which is widely used in the construction of carbon frameworks in organic chemistry.

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