6-Bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid

97%

Reagent Code: #129478
fingerprint
CAS Number 1805506-21-1

science Other reagents with same CAS 1805506-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218 g/mol
Formula C₆H₄BrNO₃
badge Registry Numbers
MDL Number MFCD30721036
thermostat Physical Properties
Boiling Point 387.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 2.015±0.06 g/cm3(Predicted)
Storage Room temperature, seal, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions to introduce the pyridone scaffold into larger molecules, enhancing binding affinity and metabolic stability in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and structural properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,530.00
inventory 250mg
10-20 days ฿14,190.00
inventory 1g
10-20 days ฿28,390.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-Bromo-2-oxo-1,2-dihydropyridine-3-carboxylic acid
No image available

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions to introduce the pyridone scaffold into larger molecules, enhancing binding affinity and metabolic stability in drug candidates. Also utilized in agroch

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for constructing nitrogen-containing heterocycles. Commonly employed in cross-coupling reactions to introduce the pyridone scaffold into larger molecules, enhancing binding affinity and metabolic stability in drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its reactivity and structural properties.

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...