2-(Hydroxymethyl)isonicotinic acid

95%

Reagent Code: #64275
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CAS Number 915140-06-6

science Other reagents with same CAS 915140-06-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.13538 g/mol
Formula C₇H₇NO₃
badge Registry Numbers
MDL Number MFCD11977439
thermostat Physical Properties
Boiling Point 478.4±35.0 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.404 g/cm3
Storage 2-8°C

description Product Description

Used in the synthesis of pharmaceuticals, particularly in the development of anti-tuberculosis drugs due to its structural similarity to isoniazid, a key compound in tuberculosis treatment. It serves as an intermediate in organic synthesis, enabling the creation of various heterocyclic compounds with potential therapeutic applications. Additionally, it is utilized in research for designing novel drug candidates targeting bacterial and fungal infections. Its hydroxyl and carboxylic acid functional groups make it versatile for chemical modifications, enhancing its role in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 10mg
10-20 days ฿3,672.00
inventory 50mg
10-20 days ฿13,950.00
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2-(Hydroxymethyl)isonicotinic acid
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Used in the synthesis of pharmaceuticals, particularly in the development of anti-tuberculosis drugs due to its structural similarity to isoniazid, a key compound in tuberculosis treatment. It serves as an intermediate in organic synthesis, enabling the creation of various heterocyclic compounds with potential therapeutic applications. Additionally, it is utilized in research for designing novel drug candidates targeting bacterial and fungal infections. Its hydroxyl and carboxylic acid functional groups

Used in the synthesis of pharmaceuticals, particularly in the development of anti-tuberculosis drugs due to its structural similarity to isoniazid, a key compound in tuberculosis treatment. It serves as an intermediate in organic synthesis, enabling the creation of various heterocyclic compounds with potential therapeutic applications. Additionally, it is utilized in research for designing novel drug candidates targeting bacterial and fungal infections. Its hydroxyl and carboxylic acid functional groups make it versatile for chemical modifications, enhancing its role in medicinal chemistry.

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