2-Ethoxyisonicotinic acid

98%

Reagent Code: #184360
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CAS Number 91940-86-2

science Other reagents with same CAS 91940-86-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 167.16 g/mol
Formula C₈H₉NO₃
badge Registry Numbers
MDL Number MFCD04115719
thermostat Physical Properties
Boiling Point 383.1 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antitubercular drugs. It serves as a key building block in the preparation of isoniazid derivatives, enhancing the efficacy and stability of active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in the production of agrochemicals and heterocyclic compounds due to its reactive carboxylic acid group and pyridine ring system.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,780.00
inventory 5g
10-20 days ฿8,550.00

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2-Ethoxyisonicotinic acid
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of antitubercular drugs. It serves as a key building block in the preparation of isoniazid derivatives, enhancing the efficacy and stability of active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in the production of agrochemicals and heterocyclic compounds due to its reactive carboxylic acid group and pyridine ring s

Used in the synthesis of pharmaceutical intermediates, particularly in the development of antitubercular drugs. It serves as a key building block in the preparation of isoniazid derivatives, enhancing the efficacy and stability of active compounds. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for optimizing drug candidates. Also employed in the production of agrochemicals and heterocyclic compounds due to its reactive carboxylic acid group and pyridine ring system.

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