Ethyl 2-Aminoisonicotinate

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Reagent Code: #182205
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CAS Number 13362-30-6

science Other reagents with same CAS 13362-30-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 166.18 g/mol
Formula C₈H₁₀N₂O₂
badge Registry Numbers
MDL Number MFCD03791260
thermostat Physical Properties
Melting Point 123.0 to 127.0 deg-C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular and antiviral agents. Its structure supports the construction of nitrogen-containing heterocyclic compounds, which are common in bioactive molecules. It is also employed in the preparation of pyridine-based derivatives for medicinal chemistry research and in the creation of ligands for catalysis. Its amino and ester functional groups allow for versatile chemical modifications, making it valuable in drug discovery and development processes.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿148.50
inventory 5g
10-20 days ฿258.50
inventory 25g
10-20 days ฿1,830.00
inventory 100g
10-20 days ฿7,170.00

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Ethyl 2-Aminoisonicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular and antiviral agents. Its structure supports the construction of nitrogen-containing heterocyclic compounds, which are common in bioactive molecules. It is also employed in the preparation of pyridine-based derivatives for medicinal chemistry research and in the creation of ligands for catalysis. Its amino and ester functional groups allow for versatile chemical modifications, making it valua

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular and antiviral agents. Its structure supports the construction of nitrogen-containing heterocyclic compounds, which are common in bioactive molecules. It is also employed in the preparation of pyridine-based derivatives for medicinal chemistry research and in the creation of ligands for catalysis. Its amino and ester functional groups allow for versatile chemical modifications, making it valuable in drug discovery and development processes.

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