5-Bromo-3-methyl-1H-pyrazolo[3,4-c]pyridine

≥97%

Reagent Code: #148509
fingerprint
CAS Number 929617-30-1

science Other reagents with same CAS 929617-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.05 g/mol
Formula C₇H₆BrN₃
badge Registry Numbers
MDL Number MFCD12024520
thermostat Physical Properties
Boiling Point 384.109°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form substituted heterocyclic structures with biological activity. Commonly employed in the preparation of potential anti-inflammatory, antiviral, and anticancer agents. Its bromo functional group allows for further cross-coupling reactions, enabling the introduction of various substituents to optimize drug potency and selectivity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,060.00
inventory 250mg
10-20 days ฿2,280.00
inventory 1g
10-20 days ฿9,070.00
inventory 5g
10-20 days ฿45,300.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
5-Bromo-3-methyl-1H-pyrazolo[3,4-c]pyridine
No image available
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form substituted heterocyclic structures with biological activity. Commonly employed in the preparation of potential anti-inflammatory, antiviral, and anticancer agents. Its bromo functional group allows for further cross-coupling reactions, enabling the introduction of various substituen
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. It serves as a building block in medicinal chemistry due to its ability to form substituted heterocyclic structures with biological activity. Commonly employed in the preparation of potential anti-inflammatory, antiviral, and anticancer agents. Its bromo functional group allows for further cross-coupling reactions, enabling the introduction of various substituents to optimize drug potency and selectivity.
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...