Methyl 4-bromo-3-fluorothiophene-2-carboxylate

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Reagent Code: #207449
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CAS Number 395664-56-9

science Other reagents with same CAS 395664-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.06 g/mol
Formula C₆H₄BrFO₂S
badge Registry Numbers
MDL Number MFCD10566744
thermostat Physical Properties
Boiling Point 267.1°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that target specific enzymes or receptors. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of fluorinated thiophene derivatives, which can enhance metabolic stability and lipophilicity in active ingredients.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,030.00

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Methyl 4-bromo-3-fluorothiophene-2-carboxylate
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that target specific enzymes or receptors. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of fluorinated thiop

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that target specific enzymes or receptors. Its structure allows for further functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to build carbon-carbon bonds in drug discovery programs. Also utilized in the preparation of fluorinated thiophene derivatives, which can enhance metabolic stability and lipophilicity in active ingredients.

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