6-bromo-2-methoxypyridin-3-amine

98%

Reagent Code: #143970
fingerprint
CAS Number 89466-18-2

science Other reagents with same CAS 89466-18-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 203.04 g/mol
Formula C₆H₇BrN₂O
badge Registry Numbers
MDL Number MFCD06738312
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, 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 creating analogs with enhanced binding affinity. Commonly employed in the preparation of agrochemicals and drug candidates targeting neurological and inflammatory conditions. The bromo and amine groups provide sites for cross-coupling reactions, enabling efficient construction of complex molecules in both research and industrial settings.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,040.00
inventory 10g
10-20 days ฿4,040.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-bromo-2-methoxypyridin-3-amine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, 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 creating analogs with enhanced binding affinity. Commonly employed in the preparation of agrochemicals and drug candidates targeting neurological and inflammatory conditions. The bromo and amine groups provide sites for cross-coupling reactions, enabl

Used as a key intermediate in the synthesis of pharmaceuticals, 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 creating analogs with enhanced binding affinity. Commonly employed in the preparation of agrochemicals and drug candidates targeting neurological and inflammatory conditions. The bromo and amine groups provide sites for cross-coupling reactions, enabling efficient construction of complex molecules in both research and industrial settings.

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...