6-bromo-3-fluoropyridine-2-carbaldehyde

97%

Reagent Code: #143971
fingerprint
CAS Number 885267-36-7

science Other reagents with same CAS 885267-36-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.00 g/mol
Formula C₆H₃BrFNO
badge Registry Numbers
MDL Number MFCD07781224
inventory_2 Storage & Handling
Storage 2-8°C

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, featuring bromine and fluorine substituents along with the carbaldehyde group, allows for selective functionalization, enhances binding to biological targets, and improves pharmacokinetic properties such as absorption and metabolic stability. This makes it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings, as well as nucleophilic substitutions, to introduce aryl, alkyl, or other groups, enabling the optimization of drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿2,200.00
inventory 5g
10-20 days ฿7,090.00
inventory 10g
10-20 days ฿10,880.00
inventory 25g
10-20 days ฿20,800.00
inventory 50g
10-20 days ฿36,800.00
inventory 100g
10-20 days ฿70,400.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
6-bromo-3-fluoropyridine-2-carbaldehyde
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, featuring bromine and fluorine substituents along with the carbaldehyde group, allows for selective functionalization, enhances binding to biological targets, and improves pharmacokinetic properties such as absorption and metabolic stability. This makes it valuable in medicinal chemistry for constructing complex heterocyclic systems.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other biologically active compounds. Its structure, featuring bromine and fluorine substituents along with the carbaldehyde group, allows for selective functionalization, enhances binding to biological targets, and improves pharmacokinetic properties such as absorption and metabolic stability. This makes it valuable in medicinal chemistry for constructing complex heterocyclic systems. Commonly employed in cross-coupling reactions such as Suzuki or Negishi couplings, as well as nucleophilic substitutions, to introduce aryl, alkyl, or other groups, enabling the optimization of drug candidates. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its ability to enhance molecular binding and stability.

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...