Ethyl 5-methylimidazo[1,2-a]pyridine-2-carboxylate

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Reagent Code: #180515
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CAS Number 67625-35-8

science Other reagents with same CAS 67625-35-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.23 g/mol
Formula C₁₁H₁₂N₂O₂
badge Registry Numbers
MDL Number MFCD02186029
thermostat Physical Properties
Melting Point 134-135 °C
inventory_2 Storage & Handling
Density 1.19±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anxiolytic and sedative agents. It serves as a building block for compounds that act as positive allosteric modulators of GABAA receptors, which are targeted in treatments for anxiety, insomnia, and epilepsy. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also employed in research settings to develop novel heterocyclic compounds with potential biological activity.

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inventory 1g
10-20 days ฿3,070.00

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Ethyl 5-methylimidazo[1,2-a]pyridine-2-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anxiolytic and sedative agents. It serves as a building block for compounds that act as positive allosteric modulators of GABAA receptors, which are targeted in treatments for anxiety, insomnia, and epilepsy. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also employed in research settings to develop novel heterocycli

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anxiolytic and sedative agents. It serves as a building block for compounds that act as positive allosteric modulators of GABAA receptors, which are targeted in treatments for anxiety, insomnia, and epilepsy. Its structure allows for efficient derivatization, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Also employed in research settings to develop novel heterocyclic compounds with potential biological activity.

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