2-Hydroxy-6-Methylisonicotinic Acid

≥98%

Reagent Code: #194916
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CAS Number 86454-13-9

science Other reagents with same CAS 86454-13-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.14 g/mol
Formula C₇H₇NO₃
badge Registry Numbers
MDL Number MFCD02682019
thermostat Physical Properties
Melting Point >300 °C
inventory_2 Storage & Handling
Density 1.345g/mL
Storage Room temperature, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in antitubercular drugs like isoniazid derivatives. It serves as a building block in medicinal chemistry due to its structural similarity to pyridine-based bioactive compounds. Also employed in the development of agrochemicals and functional materials where chelating or hydrogen-bonding properties are required. Its hydroxyl and carboxylic acid groups allow for easy modification in multi-step organic syntheses.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿2,470.00
inventory 25g
10-20 days ฿12,100.00
inventory 100g
10-20 days ฿42,840.00

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2-Hydroxy-6-Methylisonicotinic Acid
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Used in the synthesis of pharmaceutical intermediates, particularly in antitubercular drugs like isoniazid derivatives. It serves as a building block in medicinal chemistry due to its structural similarity to pyridine-based bioactive compounds. Also employed in the development of agrochemicals and functional materials where chelating or hydrogen-bonding properties are required. Its hydroxyl and carboxylic acid groups allow for easy modification in multi-step organic syntheses.

Used in the synthesis of pharmaceutical intermediates, particularly in antitubercular drugs like isoniazid derivatives. It serves as a building block in medicinal chemistry due to its structural similarity to pyridine-based bioactive compounds. Also employed in the development of agrochemicals and functional materials where chelating or hydrogen-bonding properties are required. Its hydroxyl and carboxylic acid groups allow for easy modification in multi-step organic syntheses.

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