N-Methyl-3-oxo-N-phenylbutanamide

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Reagent Code: #218986
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CAS Number 2584-48-7

science Other reagents with same CAS 2584-48-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.23 g/mol
Formula C₁₁H₁₃NO₂
badge Registry Numbers
MDL Number MFCD00129141
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functional group transformations, making it valuable in building complex molecules. Commonly employed in the development of bioactive compounds due to the presence of both amide and ketone functionalities, which can participate in various condensation and reduction reactions. Also utilized in the synthesis of heterocyclic compounds, which are prevalent in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,980.00
inventory 250mg
10-20 days ฿9,580.00
inventory 1g
10-20 days ฿19,160.00
inventory 5g
10-20 days ฿57,490.00

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N-Methyl-3-oxo-N-phenylbutanamide
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functional group transformations, making it valuable in building complex molecules. Commonly employed in the development of bioactive compounds due to the presence of both amide and ketone functionalities, which can participate in various condensation and reduction reactions. Also utilized in the synthesis of heterocyclic compounds, which are prevalent in drug disco

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its structure allows for functional group transformations, making it valuable in building complex molecules. Commonly employed in the development of bioactive compounds due to the presence of both amide and ketone functionalities, which can participate in various condensation and reduction reactions. Also utilized in the synthesis of heterocyclic compounds, which are prevalent in drug discovery programs.

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