3-Bromo-6-methoxy-2,4-dimethylpyridine

95%

Reagent Code: #145075
fingerprint
CAS Number 819069-57-3

science Other reagents with same CAS 819069-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.08 g/mol
Formula C₈H₁₀BrNO
thermostat Physical Properties
Boiling Point 243°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to build complex aromatic systems. Also utilized in agrochemical research for designing new active ingredients in crop protection agents. Its bromine moiety facilitates easy substitution, enabling efficient derivatization in multi-step organic syntheses.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿6,900.00
inventory 25mg
10-20 days ฿3,070.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
3-Bromo-6-methoxy-2,4-dimethylpyridine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to build complex aromatic systems. Also utilized in agrochemical research for designing new active ingredients in crop protection

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure allows for selective functionalization, making it valuable in medicinal chemistry for creating compounds with high target specificity. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings to build complex aromatic systems. Also utilized in agrochemical research for designing new active ingredients in crop protection agents. Its bromine moiety facilitates easy substitution, enabling efficient derivatization in multi-step organic syntheses.

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...