Ethyl 2-hydroxy-6-methylisonicotinate

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Reagent Code: #180634
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CAS Number 150190-03-7

science Other reagents with same CAS 150190-03-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 181.19 g/mol
Formula C₉H₁₁NO₃
badge Registry Numbers
MDL Number MFCD09953494
thermostat Physical Properties
Melting Point 188-190 °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 drugs. It serves as a building block for pyridine-based compounds that exhibit biological activity against Mycobacterium tuberculosis. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in the preparation of agrochemicals and specialty heterocyclic compounds due to its reactive hydroxy and ester groups.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,710.00
inventory 1g
10-20 days ฿12,710.00
inventory 5g
10-20 days ฿44,450.00

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Ethyl 2-hydroxy-6-methylisonicotinate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular drugs. It serves as a building block for pyridine-based compounds that exhibit biological activity against Mycobacterium tuberculosis. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in the preparation of agrochemicals and specialty heterocyclic compounds due to its reactive hydroxy and ester groups.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of antitubercular drugs. It serves as a building block for pyridine-based compounds that exhibit biological activity against Mycobacterium tuberculosis. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in the preparation of agrochemicals and specialty heterocyclic compounds due to its reactive hydroxy and ester groups.

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