3-Chloro-2-hydrazinopyridine

98%

Reagent Code: #159376
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CAS Number 22841-92-5

science Other reagents with same CAS 22841-92-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.58 g/mol
Formula C₅H₆ClN₃
badge Registry Numbers
MDL Number MFCD01936479
thermostat Physical Properties
Melting Point 165-167 °C
Boiling Point 276.7 °C at 760 mmHg
inventory_2 Storage & Handling
Storage -20°C, Inert gas, Light-proof

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block for heterocyclic compounds due to its reactive hydrazine and pyridine groups. Commonly employed in the preparation of pyridopyrimidines and other fused ring systems with biological activity. Also utilized in agrochemical research for developing novel pesticides and herbicides. Its ability to form hydrazone derivatives makes it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿300.00
inventory 25g
10-20 days ฿670.00
inventory 500g
10-20 days ฿8,650.00
inventory 100g
10-20 days ฿2,000.00

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3-Chloro-2-hydrazinopyridine
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block for heterocyclic compounds due to its reactive hydrazine and pyridine groups. Commonly employed in the preparation of pyridopyrimidines and other fused ring systems with biological activity. Also utilized in agrochemical research for developing novel pesticides and herbicides. Its ability to form hydrazone derivatives makes it valuable in m

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular and antimicrobial agents. It serves as a building block for heterocyclic compounds due to its reactive hydrazine and pyridine groups. Commonly employed in the preparation of pyridopyrimidines and other fused ring systems with biological activity. Also utilized in agrochemical research for developing novel pesticides and herbicides. Its ability to form hydrazone derivatives makes it valuable in medicinal chemistry for structure-activity relationship studies.

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