Methyl 5-Bromo-3-Methylfuran-2-Carboxylate

95%

Reagent Code: #209689
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CAS Number 2528-01-0

science Other reagents with same CAS 2528-01-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.03 g/mol
Formula C₇H₇BrO₃
badge Registry Numbers
MDL Number MFCD06227465
inventory_2 Storage & Handling
Storage Room temperature, airtight, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with furan ring systems. Its bromo and ester functional groups allow for further chemical modifications, making it valuable in constructing complex organic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the preparation of heterocyclic compounds with potential antimicrobial or anti-inflammatory properties. Its versatility in organic synthesis makes it a preferred building block in medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,340.00
inventory 1g
10-20 days ฿26,000.00
inventory 250mg
10-20 days ฿8,670.00
Methyl 5-Bromo-3-Methylfuran-2-Carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with furan ring systems. Its bromo and ester functional groups allow for further chemical modifications, making it valuable in constructing complex organic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the preparation of heterocyclic compounds with potential antimicrobial or anti-i

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules with furan ring systems. Its bromo and ester functional groups allow for further chemical modifications, making it valuable in constructing complex organic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Heck reactions to form carbon-carbon bonds. Also utilized in the preparation of heterocyclic compounds with potential antimicrobial or anti-inflammatory properties. Its versatility in organic synthesis makes it a preferred building block in medicinal chemistry research.

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