Methyl 4-methylnicotinate

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Reagent Code: #206399
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CAS Number 33402-75-4

science Other reagents with same CAS 33402-75-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 151.16 g/mol
Formula C₈H₉NO₂
thermostat Physical Properties
Boiling Point 215.2°C
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential biological activity. It serves as a building block in medicinal chemistry for creating compounds that may exhibit anti-inflammatory, antihypertensive, or neuroactive properties. Also utilized in research settings for the preparation of heterocyclic compounds and in the optimization of drug candidates through structural modification. Its ester functionality allows for easy transformation into amides or carboxylic acids, enabling further chemical elaboration in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿490.00
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿3,560.00
inventory 25g
10-20 days ฿11,340.00
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Methyl 4-methylnicotinate
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Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential biological activity. It serves as a building block in medicinal chemistry for creating compounds that may exhibit anti-inflammatory, antihypertensive, or neuroactive properties. Also utilized in research settings for the preparation of heterocyclic compounds and in the optimization of drug candidates through structural modification. Its ester functionality allows for e

Used as an intermediate in the synthesis of pharmaceuticals, particularly in the development of nicotinic acid derivatives with potential biological activity. It serves as a building block in medicinal chemistry for creating compounds that may exhibit anti-inflammatory, antihypertensive, or neuroactive properties. Also utilized in research settings for the preparation of heterocyclic compounds and in the optimization of drug candidates through structural modification. Its ester functionality allows for easy transformation into amides or carboxylic acids, enabling further chemical elaboration in synthetic pathways.

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