Imidazo[1,2-a]pyridin-6-ylmethanol

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Reagent Code: #200252
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CAS Number 132213-07-1

science Other reagents with same CAS 132213-07-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 148.16 g/mol
Formula C₈H₈N₂O
badge Registry Numbers
MDL Number MFCD07368521
thermostat Physical Properties
Melting Point 106-108°C
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anxiolytic and sedative agents. It serves as a building block for modulating GABA receptors due to its structural similarity to known bioactive molecules. Its hydroxyl group allows for easy functionalization, enabling the creation of esters, ethers, or conjugates to enhance drug potency or bioavailability. Commonly employed in medicinal chemistry for optimizing lead compounds in central nervous system (CNS) drug discovery programs. Also explored in the preparation of kinase inhibitors and antimicrobial agents due to its favorable binding properties with biological targets.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿3,320.00
inventory 5g
10-20 days ฿16,250.00
inventory 10g
10-20 days ฿24,020.00

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Imidazo[1,2-a]pyridin-6-ylmethanol
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anxiolytic and sedative agents. It serves as a building block for modulating GABA receptors due to its structural similarity to known bioactive molecules. Its hydroxyl group allows for easy functionalization, enabling the creation of esters, ethers, or conjugates to enhance drug potency or bioavailability. Commonly employed in medicinal chemistry for optimizing lead compounds in central nervous system
Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of anxiolytic and sedative agents. It serves as a building block for modulating GABA receptors due to its structural similarity to known bioactive molecules. Its hydroxyl group allows for easy functionalization, enabling the creation of esters, ethers, or conjugates to enhance drug potency or bioavailability. Commonly employed in medicinal chemistry for optimizing lead compounds in central nervous system (CNS) drug discovery programs. Also explored in the preparation of kinase inhibitors and antimicrobial agents due to its favorable binding properties with biological targets.
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