Methyl 1H-Pyrazolo[3,4-B]Pyridine-3-Carboxylate

≥97%

Reagent Code: #214350
fingerprint
CAS Number 916325-83-2

science Other reagents with same CAS 916325-83-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.16 g/mol
Formula C₈H₇N₃O₂
badge Registry Numbers
MDL Number MFCD13176786
thermostat Physical Properties
Boiling Point 369.0±22.0 °C
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports the design of drugs targeting inflammatory diseases, cancer, and central nervous system disorders. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for developing new crop protection agents due to its favorable reactivity and stability in synthetic pathways.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,560.00
inventory 5g
10-20 days ฿28,320.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
Methyl 1H-Pyrazolo[3,4-B]Pyridine-3-Carboxylate
No image available

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports the design of drugs targeting inflammatory diseases, cancer, and central nervous system disorders. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for developing new crop protection agents due to its favorable reactivity and sta

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Its structure supports the design of drugs targeting inflammatory diseases, cancer, and central nervous system disorders. Commonly employed in medicinal chemistry for scaffold modification to enhance drug potency and selectivity. Also utilized in agrochemical research for developing new crop protection agents due to its favorable reactivity and stability in synthetic pathways.

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...