2-Bromo-6-pyrrolidin-1-ylpyridine

98%

Reagent Code: #149111
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CAS Number 230618-41-4

science Other reagents with same CAS 230618-41-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 227.101 g/mol
Formula C₉H₁₁BrN₂
badge Registry Numbers
MDL Number MFCD08271892
thermostat Physical Properties
Melting Point 86 °C
Boiling Point 335.49 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

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 medicinal chemistry due to its ability to form stable, biologically active structures. Commonly employed in the preparation of compounds targeting neurological disorders and inflammatory diseases. Its bromo and pyrrolidinyl functional groups allow for selective cross-coupling reactions, making it valuable in creating diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing novel pesticides with improved selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,040.00

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2-Bromo-6-pyrrolidin-1-ylpyridine
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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 medicinal chemistry due to its ability to form stable, biologically active structures. Commonly employed in the preparation of compounds targeting neurological disorders and inflammatory diseases. Its bromo and pyrrolidinyl functional groups allow for selective cross-coupling reactions, making it valuable in creating diverse compound l

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 medicinal chemistry due to its ability to form stable, biologically active structures. Commonly employed in the preparation of compounds targeting neurological disorders and inflammatory diseases. Its bromo and pyrrolidinyl functional groups allow for selective cross-coupling reactions, making it valuable in creating diverse compound libraries for drug discovery. Also utilized in agrochemical research for designing novel pesticides with improved selectivity.

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