6-Bromo-5-methyl-1H-imidazo[4,5-b]pyridine

≥95%

Reagent Code: #148459
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CAS Number 28279-41-6

science Other reagents with same CAS 28279-41-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 212.05 g/mol
Formula C₇H₆BrN₃
badge Registry Numbers
MDL Number MFCD00184166
thermostat Physical Properties
Boiling Point 230.6±50.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.755g/cm3
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating targeted therapies. Commonly employed in research settings to build more complex heterocyclic systems with biological activity. Also utilized in the preparation of receptor antagonists and modulators in neuropharmacology. Due to its bromine functionality, it readily undergoes cross-coupling reactions, enabling efficient construction of drug-like molecules in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,600.00
inventory 250mg
10-20 days ฿9,200.00

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6-Bromo-5-methyl-1H-imidazo[4,5-b]pyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating targeted therapies. Commonly employed in research settings to build more complex heterocyclic systems with biological activity. Also utilized in the preparation of receptor antagonists and modulators in neuropharmacology. Due to its bromine functionality, it readily undergoes cros

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its structure allows for selective modification, making it valuable in creating targeted therapies. Commonly employed in research settings to build more complex heterocyclic systems with biological activity. Also utilized in the preparation of receptor antagonists and modulators in neuropharmacology. Due to its bromine functionality, it readily undergoes cross-coupling reactions, enabling efficient construction of drug-like molecules in medicinal chemistry.

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