N-(tert-Butyl)-6-chloro-4-(o-tolyl)nicotinamide

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Reagent Code: #124819
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CAS Number 342417-04-3

science Other reagents with same CAS 342417-04-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.80 g/mol
Formula C₁₇H₁₉ClN₂O
badge Registry Numbers
MDL Number MFCD09032565
thermostat Physical Properties
Boiling Point 429.4±45.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of pharmaceutical agents, particularly those targeting specific enzymes or receptors in the body. Its structure, featuring a nicotinamide core, makes it a valuable building block for creating compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, or antiviral properties. Researchers also explore its use in designing inhibitors for various biological pathways, contributing to drug discovery and development efforts. Additionally, its chemical properties allow for further functionalization, enabling the creation of derivatives with enhanced biological activity or selectivity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿378.00
inventory 1g
10-20 days ฿1,089.00

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N-(tert-Butyl)-6-chloro-4-(o-tolyl)nicotinamide
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This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of more complex molecules. It is often employed in the development of pharmaceutical agents, particularly those targeting specific enzymes or receptors in the body. Its structure, featuring a nicotinamide core, makes it a valuable building block for creating compounds with potential therapeutic effects, such as anti-inflammatory, anticancer, or antiviral properties. Researchers also explore its use in designing inhibitors for various biological pathways, contributing to drug discovery and development efforts. Additionally, its chemical properties allow for further functionalization, enabling the creation of derivatives with enhanced biological activity or selectivity.
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