4-Bromo-5-Methoxypyridin-2(1H)-One

95%

Reagent Code: #154015
fingerprint
CAS Number 1630197-34-0

science Other reagents with same CAS 1630197-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.02 g/mol
Formula C₆H₆BrNO₂
inventory_2 Storage & Handling
Storage Room temperature

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 targeting neurological and inflammatory disorders. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups, enhancing molecular diversity. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and environmental profiles.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿6,480.00
250mg
10-20 days ฿12,240.00
500mg
10-20 days ฿21,960.00
1g
10-20 days ฿32,280.00
4-Bromo-5-Methoxypyridin-2(1H)-One
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting neurological and inflammatory disorders. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups, enhancing molecular diversity. Als

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and other bioactive molecules targeting neurological and inflammatory disorders. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for building pyridine-based drug candidates. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig aminations to introduce aryl or amine groups, enhancing molecular diversity. Also utilized in agrochemical research for designing novel pesticides with improved selectivity and environmental profiles.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...