Methyl 2-bromo-3-methylbut-2-enoate

95%

Reagent Code: #203388
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CAS Number 51263-40-2

science Other reagents with same CAS 51263-40-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.04 g/mol
Formula C₆H₉BrO₂
badge Registry Numbers
MDL Number MFCD14702516
inventory_2 Storage & Handling
Storage -20°C, Inert Gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its α,β-unsaturated ester structure with a bromine substituent makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. It is also employed in the synthesis of complex natural products and bioactive molecules due to its reactivity as a Michael acceptor. The compound's versatility allows for functionalization at multiple sites, facilitating the construction of diverse molecular frameworks in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,800.00
inventory 250mg
10-20 days ฿25,930.00
inventory 1g
10-20 days ฿82,970.00
Methyl 2-bromo-3-methylbut-2-enoate
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Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its α,β-unsaturated ester structure with a bromine substituent makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. It is also employed in the synthesis of complex natural products and bioactive molecules due to its reactivity as a Michael acceptor. The compound's versatility allows for functionalization at multip

Used as a key intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its α,β-unsaturated ester structure with a bromine substituent makes it valuable in cross-coupling reactions, such as Suzuki or Heck reactions, enabling the formation of carbon-carbon bonds. It is also employed in the synthesis of complex natural products and bioactive molecules due to its reactivity as a Michael acceptor. The compound's versatility allows for functionalization at multiple sites, facilitating the construction of diverse molecular frameworks in medicinal chemistry research.

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