2-Bromo-6-iodo-3-methoxypyridine

95%

Reagent Code: #43367
fingerprint
CAS Number 321535-37-9

science Other reagents with same CAS 321535-37-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.93 g/mol
Formula C₆H₅BrINO
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas, protected from light

description Product Description

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Stille couplings, due to the presence of both bromine and iodine atoms, which act as reactive sites for these transformations. The methoxy group further enhances its reactivity and selectivity in various chemical processes. It is commonly used in pharmaceutical research for the synthesis of drug intermediates, particularly in the development of compounds with potential therapeutic applications. Additionally, it finds use in material science for creating specialized organic compounds with unique electronic or structural properties.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,107.00
inventory 1g
10-20 days ฿2,790.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Bromo-6-iodo-3-methoxypyridine
No image available

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Stille couplings, due to the presence of both bromine and iodine atoms, which act as reactive sites for these transformations. The methoxy group further enhances its reactivity and selectivity in various chemical processes. It is commonly used in pharmaceutical research for the synthesis of drug intermedia

This chemical is primarily utilized in organic synthesis as a versatile building block for the development of more complex molecules. It is often employed in cross-coupling reactions, such as Suzuki or Stille couplings, due to the presence of both bromine and iodine atoms, which act as reactive sites for these transformations. The methoxy group further enhances its reactivity and selectivity in various chemical processes. It is commonly used in pharmaceutical research for the synthesis of drug intermediates, particularly in the development of compounds with potential therapeutic applications. Additionally, it finds use in material science for creating specialized organic compounds with unique electronic or 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...