Ethyl 8-bromo-1,6-naphthyridine-3-carboxylate

97%

Reagent Code: #184495
fingerprint
CAS Number 2089652-13-9

science Other reagents with same CAS 2089652-13-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.11 g/mol
Formula C₁₁H₉BrN₂O₂
badge Registry Numbers
MDL Number MFCD30828915
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antimicrobial compounds. Its structure supports functionalization at multiple sites, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, enabling the creation of diverse compound libraries for biological screening. Also utilized in the preparation of fluorescent probes due to the inherent photophysical properties of the naphthyridine core.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿27,330.00
inventory 250mg
10-20 days ฿43,600.00
inventory 1g
10-20 days ฿113,210.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Ethyl 8-bromo-1,6-naphthyridine-3-carboxylate
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antimicrobial compounds. Its structure supports functionalization at multiple sites, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, enabling the creation of diverse compound libraries for biological screening. Also utili

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and antimicrobial compounds. Its structure supports functionalization at multiple sites, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce aryl or amino groups, enabling the creation of diverse compound libraries for biological screening. Also utilized in the preparation of fluorescent probes due to the inherent photophysical properties of the naphthyridine core.

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...