2-Hydrazinyl-3-methoxypyridine

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Reagent Code: #196984
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CAS Number 210992-34-0

science Other reagents with same CAS 210992-34-0

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Weight 139.16 g/mol
Formula C₆H₉N₃O
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MDL Number MFCD09999917
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridine-based drugs with biological activity. It serves in the preparation of heterocyclic compounds for potential use in antiviral and antitumor agents. Also employed in agrochemical research for designing novel pesticides and herbicides due to its reactive hydrazine group. Commonly utilized in organic synthesis to build complex nitrogen-containing rings through cyclization reactions. Its methoxy and hydrazine functionalities allow for selective modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿8,320.00
inventory 1g
10-20 days ฿15,380.00

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2-Hydrazinyl-3-methoxypyridine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridine-based drugs with biological activity. It serves in the preparation of heterocyclic compounds for potential use in antiviral and antitumor agents. Also employed in agrochemical research for designing novel pesticides and herbicides due to its reactive hydrazine group. Commonly utilized in organic synthesis to build complex nitrogen-containing rings through cyclization reactions. Its methoxy and hydr

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of pyridine-based drugs with biological activity. It serves in the preparation of heterocyclic compounds for potential use in antiviral and antitumor agents. Also employed in agrochemical research for designing novel pesticides and herbicides due to its reactive hydrazine group. Commonly utilized in organic synthesis to build complex nitrogen-containing rings through cyclization reactions. Its methoxy and hydrazine functionalities allow for selective modifications, making it valuable in medicinal chemistry for structure-activity relationship studies.

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