5-Bromo-2-iodoisonicotinaldehyde

97%

Reagent Code: #48946
fingerprint
CAS Number 1289018-37-6

science Other reagents with same CAS 1289018-37-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 311.9026 g/mol
Formula C₆H₃BrINO
inventory_2 Storage & Handling
Storage room temperature

description Product Description

Used in organic synthesis as a versatile building block for the development of complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential biological activities. The presence of both bromo and iodo substituents allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse chemical structures. Its aldehyde group also provides a reactive site for further derivatization, making it valuable in the design of drug candidates and agrochemicals. Additionally, it is employed in the synthesis of ligands for catalysis and materials science applications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,106.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-2-iodoisonicotinaldehyde
No image available

Used in organic synthesis as a versatile building block for the development of complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential biological activities. The presence of both bromo and iodo substituents allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse chemical structures. Its ald

Used in organic synthesis as a versatile building block for the development of complex molecules, particularly in pharmaceutical research. It serves as a key intermediate in the preparation of heterocyclic compounds, which are often explored for their potential biological activities. The presence of both bromo and iodo substituents allows for selective functionalization through cross-coupling reactions, such as Suzuki or Sonogashira couplings, enabling the creation of diverse chemical structures. Its aldehyde group also provides a reactive site for further derivatization, making it valuable in the design of drug candidates and agrochemicals. Additionally, it is employed in the synthesis of ligands for catalysis and materials science applications.

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...