Methyl 2-(2-bromothiophen-3-yl)acetate

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Reagent Code: #62308
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CAS Number 683251-61-8

science Other reagents with same CAS 683251-61-8

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scatter_plot Molecular Information
Weight 235.1 g/mol
Formula C₇H₇BrO₂S
badge Registry Numbers
MDL Number MFCD27927327
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its bromothiophene moiety makes it valuable for coupling reactions, such as Suzuki or Sonogashira cross-coupling, which are essential for creating biologically active compounds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often used in drug discovery and material science. Its ester functional group allows for further chemical modifications, making it versatile in various synthetic pathways.

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inventory 10mg
10-20 days ฿4,527.00

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Methyl 2-(2-bromothiophen-3-yl)acetate
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This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its bromothiophene moiety makes it valuable for coupling reactions, such as Suzuki or Sonogashira cross-coupling, which are essential for creating biologically active compounds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often used in drug discove
This chemical is primarily utilized in organic synthesis, particularly in the construction of complex molecules. It serves as a key intermediate in the development of pharmaceuticals, agrochemicals, and other fine chemicals. Its bromothiophene moiety makes it valuable for coupling reactions, such as Suzuki or Sonogashira cross-coupling, which are essential for creating biologically active compounds. Additionally, it is employed in the synthesis of heterocyclic compounds, which are often used in drug discovery and material science. Its ester functional group allows for further chemical modifications, making it versatile in various synthetic pathways.
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