7-Bromofuro[3,2-c]pyridine

98%

Reagent Code: #153433
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CAS Number 603300-96-5

science Other reagents with same CAS 603300-96-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.02 g/mol
Formula C₇H₄BrNO
badge Registry Numbers
MDL Number MFCD18254548
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the optimization of drug candidates with improved potency and selectivity. Also utilized in agrochemical research for designing novel active ingredients with enhanced stability and activity.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿7,180.00
inventory 100mg
10-20 days ฿12,190.00
inventory 250mg
10-20 days ฿21,780.00
inventory 1g
10-20 days ฿68,560.00

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7-Bromofuro[3,2-c]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the optimization of drug candidates with improved potency and selectivity

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amino groups, enabling the optimization of drug candidates with improved potency and selectivity. Also utilized in agrochemical research for designing novel active ingredients with enhanced stability and activity.

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