Methyl 6-bromo-5-fluoropyridine-3-carboxylate

98%

Reagent Code: #205771
fingerprint
CAS Number 1214336-88-5

science Other reagents with same CAS 1214336-88-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.02 g/mol
Formula C₇H₅BrFNO₂
badge Registry Numbers
MDL Number MFCD14698110
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

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 constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce the pyridine core into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic system and ease of derivatization.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿850.00
inventory 1g
10-20 days ฿1,590.00
inventory 5g
10-20 days ฿7,600.00
inventory 25g
10-20 days ฿37,600.00
inventory 50g
10-20 days ฿73,600.00
inventory 10g
10-20 days ฿15,120.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 6-bromo-5-fluoropyridine-3-carboxylate
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 constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce the pyridine core into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbici

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 constructing complex heterocyclic compounds. Commonly employed in cross-coupling reactions such as Suzuki or Buchwald-Hartwig to introduce the pyridine core into target molecules. Also utilized in agrochemical research for designing novel pesticides and herbicides due to its electron-deficient aromatic system and ease of derivatization.

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...