3-Bromo-2-iodo-5-methylpyridine

97%

Reagent Code: #154483
fingerprint
CAS Number 1211542-16-3

science Other reagents with same CAS 1211542-16-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.92 g/mol
Formula C₆H₅BrIN
badge Registry Numbers
MDL Number MFCD16610048
inventory_2 Storage & Handling
Storage 2-8°C, Sealed, Dry, Light-proof, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance potency and selectivity. Also utilized in the preparation of functionalized heterocycles for use in crop protection agents and drug candidates targeting inflammatory and oncological diseases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿8,170.00
250mg
10-20 days ฿13,870.00
1g
10-20 days ฿45,950.00
3-Bromo-2-iodo-5-methylpyridine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance potency and selectivity. Also utilized in the preparation of functionalized heterocycles

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other biologically active compounds. Its halogen substituents allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex molecules. Commonly employed in medicinal chemistry for modifying pyridine-based scaffolds to enhance potency and selectivity. Also utilized in the preparation of functionalized heterocycles for use in crop protection agents and drug candidates targeting inflammatory and oncological diseases.

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...