2-Amino-3-pyridinecarboxaldehyde

97%

Reagent Code: #134844
label
Alias 2-amino-3-pyridine formaldehyde; 2-amino-3-aldehyde pyridine
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CAS Number 7521-41-7

science Other reagents with same CAS 7521-41-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 122.12 g/mol
Formula C₆H₆N₂O
badge Registry Numbers
MDL Number MFCD01830382
thermostat Physical Properties
Melting Point 98-102 °C(lit.)
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of antitubercular and antiviral agents. It serves as a building block in the development of pyridine-based drug candidates due to its reactive amino and aldehyde functional groups, which allow for easy modification and ring formation. Commonly employed in the preparation of fused heterocyclic compounds such as imidazopyridines and triazolopyridines, which exhibit biological activity. Also utilized in agrochemical research for developing novel pesticides and herbicides. Its ability to form Schiff bases makes it valuable in coordination chemistry for creating metal-organic frameworks and catalysts.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿1,050.00
inventory 25g
10-20 days ฿5,200.00

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2-Amino-3-pyridinecarboxaldehyde
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Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of antitubercular and antiviral agents. It serves as a building block in the development of pyridine-based drug candidates due to its reactive amino and aldehyde functional groups, which allow for easy modification and ring formation. Commonly employed in the preparation of fused heterocyclic compounds such as imidazopyridines and triazolopyridines, which exhibit biological activity. Also utilized in ag

Used as a key intermediate in the synthesis of various pharmaceuticals, particularly in the production of antitubercular and antiviral agents. It serves as a building block in the development of pyridine-based drug candidates due to its reactive amino and aldehyde functional groups, which allow for easy modification and ring formation. Commonly employed in the preparation of fused heterocyclic compounds such as imidazopyridines and triazolopyridines, which exhibit biological activity. Also utilized in agrochemical research for developing novel pesticides and herbicides. Its ability to form Schiff bases makes it valuable in coordination chemistry for creating metal-organic frameworks and catalysts.

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