(2-Bromo-5-fluoropyridin-3-yl)methanamine hydrochloride

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Reagent Code: #152834
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CAS Number 1428532-95-9

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 241.5 g/mol
Formula C₆H₇BrClFN₂
inventory_2 Storage & Handling
Storage 2-8°C, 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. Its structure allows for selective binding in biological systems, making it valuable in creating targeted therapies. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates due to its reactive amine group and halogen moieties, which enable further functionalization. Also utilized in the preparation of antidepressants and antiviral agents through coupling reactions and nucleophilic substitutions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,600.00
inventory 250mg
10-20 days ฿6,250.00

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(2-Bromo-5-fluoropyridin-3-yl)methanamine hydrochloride
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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 binding in biological systems, making it valuable in creating targeted therapies. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates due to its reactive amine group and halogen moieties, which enable further functionalization. Also utilized in the preparation of antidepressants and antiv

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 binding in biological systems, making it valuable in creating targeted therapies. Commonly employed in medicinal chemistry for constructing pyridine-based drug candidates due to its reactive amine group and halogen moieties, which enable further functionalization. Also utilized in the preparation of antidepressants and antiviral agents through coupling reactions and nucleophilic substitutions.

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