N-(3-Methoxyphenyl)pivalamide

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Reagent Code: #218116
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CAS Number 56619-93-3

science Other reagents with same CAS 56619-93-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.27 g/mol
Formula C₁₂H₁₇NO₂
badge Registry Numbers
MDL Number MFCD00662896
thermostat Physical Properties
Boiling Point 358.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry seal

description Product Description

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the creation of complex molecules by serving as a building block in amide coupling reactions. The methoxyphenyl group enhances electron donation, influencing reactivity and selectivity in synthetic pathways. Commonly employed in research settings for designing bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Also utilized in the preparation of specialty polymers and ligands for catalysis due to its stability and steric bulk.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,650.00
inventory 5g
10-20 days ฿5,810.00
inventory 10g
10-20 days ฿8,610.00
inventory 25g
10-20 days ฿21,490.00

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N-(3-Methoxyphenyl)pivalamide
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Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the creation of complex molecules by serving as a building block in amide coupling reactions. The methoxyphenyl group enhances electron donation, influencing reactivity and selectivity in synthetic pathways. Commonly employed in research settings for designing bioactive compounds, including potential drug candidates targeting central nervous system disorders and infla

Used as an intermediate in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. Its structure supports the creation of complex molecules by serving as a building block in amide coupling reactions. The methoxyphenyl group enhances electron donation, influencing reactivity and selectivity in synthetic pathways. Commonly employed in research settings for designing bioactive compounds, including potential drug candidates targeting central nervous system disorders and inflammation. Also utilized in the preparation of specialty polymers and ligands for catalysis due to its stability and steric bulk.

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