2-Ethyl-2-phenylmalonamide

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Reagent Code: #180799
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CAS Number 7206-76-0

science Other reagents with same CAS 7206-76-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.24 g/mol
Formula C₁₁H₁₄N₂O₂
badge Registry Numbers
MDL Number MFCD00008012
inventory_2 Storage & Handling
Storage 2-8°C, Sealed

description Product Description

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. It has been explored in the development of central nervous system agents due to its structural similarity to certain sedative-hypnotic compounds. Additionally, it serves as a building block in the synthesis of heterocyclic systems, which are common in medicinal chemistry. Its amide groups can participate in hydrogen bonding, useful in crystal engineering and supramolecular chemistry applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿30,110.00

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2-Ethyl-2-phenylmalonamide
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Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. It has been explored in the development of central nervous system agents due to its structural similarity to certain sedative-hypnotic compounds. Additionally, it serves as a building block in the synthesis of heterocyclic systems, which are common in

Used primarily as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and biologically active compounds. Its structure allows for functionalization at multiple sites, making it valuable in constructing complex molecules. It has been explored in the development of central nervous system agents due to its structural similarity to certain sedative-hypnotic compounds. Additionally, it serves as a building block in the synthesis of heterocyclic systems, which are common in medicinal chemistry. Its amide groups can participate in hydrogen bonding, useful in crystal engineering and supramolecular chemistry applications.

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