Methyl 6-aminopyridine-2-carboxylate

98%

Reagent Code: #205520
fingerprint
CAS Number 36052-26-3

science Other reagents with same CAS 36052-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 152.15 g/mol
Formula C₇H₈N₂O₂
badge Registry Numbers
MDL Number MFCD00233712
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex heterocyclic compounds, making it valuable in medicinal chemistry for drug discovery. Also employed in research settings to prepare fluorescent probes and functionalized ligands for catalysis. The amine and ester groups allow for versatile chemical modifications, enabling its use in peptide-like coupling reactions and the construction of nitrogen-containing scaffolds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿159.50
inventory 5g
10-20 days ฿700.00
inventory 25g
10-20 days ฿2,550.00
inventory 100g
10-20 days ฿10,150.00
inventory 500g
10-20 days ฿50,750.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 6-aminopyridine-2-carboxylate
No image available

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex heterocyclic compounds, making it valuable in medicinal chemistry for drug discovery. Also employed in research settings to prepare fluorescent probes and functionalized ligands for catalysis. The amine and ester groups allow for versatile chemical modifications, enabling its use in peptide-like coupling reactions

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors and other bioactive molecules. Its structure supports the formation of complex heterocyclic compounds, making it valuable in medicinal chemistry for drug discovery. Also employed in research settings to prepare fluorescent probes and functionalized ligands for catalysis. The amine and ester groups allow for versatile chemical modifications, enabling its use in peptide-like coupling reactions and the construction of nitrogen-containing scaffolds.

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...