5-Bromo-2-hydrazinyl-3-methylpyridine

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Reagent Code: #131601
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CAS Number 1216259-76-5

science Other reagents with same CAS 1216259-76-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.05 g/mol
Formula C₆H₈BrN₃
badge Registry Numbers
MDL Number MFCD09999951
thermostat Physical Properties
Boiling Point 249.0±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.70±0.1 g/cm3(Predicted)
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its hydrazine and bromo functional groups allow for selective derivatization, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for scaffold modification and library generation in drug discovery programs. Also utilized in the preparation of pyridine-based ligands for metal-catalyzed reactions, supporting applications in catalysis and materials science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,260.00
inventory 250mg
10-20 days ฿12,340.00
inventory 1g
10-20 days ฿33,320.00

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5-Bromo-2-hydrazinyl-3-methylpyridine
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its hydrazine and bromo functional groups allow for selective derivatization, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for scaffold modification and library generation in drug discovery programs. Also utilized in the preparation of pyridine-based ligands for metal-catalyze

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors and antitumor agents. Its hydrazine and bromo functional groups allow for selective derivatization, enabling the construction of complex heterocyclic systems found in bioactive molecules. Commonly employed in medicinal chemistry for scaffold modification and library generation in drug discovery programs. Also utilized in the preparation of pyridine-based ligands for metal-catalyzed reactions, supporting applications in catalysis and materials science.

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