4-Bromo-1H-pyrazolo[3,4-b]pyridine

97%

Reagent Code: #145009
fingerprint
CAS Number 856859-49-9

science Other reagents with same CAS 856859-49-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 198.02 g/mol
Formula C₆H₄BrN₃
thermostat Physical Properties
Boiling Point 209°C
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 for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to its ability to undergo cross-coupling reactions, such as Suzuki and Buchwald-Hartwig aminations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies in drug discovery programs targeting inflammatory diseases and central nervous system disorders. Also utilized in the fabrication of organic semiconductors and optoelectronic materials owing to its nitrogen-rich heterocyclic structure.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿2,960.00
inventory 25g
10-20 days ฿53,040.00
inventory 5g
10-20 days ฿13,240.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
4-Bromo-1H-pyrazolo[3,4-b]pyridine
No image available

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to its ability to undergo cross-coupling reactions, such as Suzuki and Buchwald-Hartwig aminations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies in drug discovery programs targeting inflammatory diseases and central nervous system disorde

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in the preparation of biologically active compounds due to its ability to undergo cross-coupling reactions, such as Suzuki and Buchwald-Hartwig aminations. Commonly employed in medicinal chemistry for structure-activity relationship (SAR) studies in drug discovery programs targeting inflammatory diseases and central nervous system disorders. Also utilized in the fabrication of organic semiconductors and optoelectronic materials owing to its nitrogen-rich heterocyclic structure.

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...