Ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate

≥95%

Reagent Code: #183720
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CAS Number 62135-58-4

science Other reagents with same CAS 62135-58-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.19 g/mol
Formula C₉H₉N₃O₂
badge Registry Numbers
MDL Number MFCD11977822
inventory_2 Storage & Handling
Density 1.33g/cm3
Storage Store in an inert gas at room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and anxiolytic drugs. Its structure supports the formation of biologically active molecules by serving as a scaffold in heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing triazolopyridine-based compounds that exhibit high binding affinity to various receptors, including GABA receptors. Also utilized in research settings for generating novel analogs in drug discovery programs targeting neurological disorders. Its ester functionality allows for easy modification, making it valuable in combinatorial chemistry and parallel synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,650.00
inventory 250mg
10-20 days ฿14,110.00

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Ethyl [1,2,4]triazolo[1,5-a]pyridine-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and anxiolytic drugs. Its structure supports the formation of biologically active molecules by serving as a scaffold in heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing triazolopyridine-based compounds that exhibit high binding affinity to various receptors, including GABA receptors. Also utilized in research settings for generating novel

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents and anxiolytic drugs. Its structure supports the formation of biologically active molecules by serving as a scaffold in heterocyclic chemistry. Commonly employed in medicinal chemistry for constructing triazolopyridine-based compounds that exhibit high binding affinity to various receptors, including GABA receptors. Also utilized in research settings for generating novel analogs in drug discovery programs targeting neurological disorders. Its ester functionality allows for easy modification, making it valuable in combinatorial chemistry and parallel synthesis.

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