1-(3-Aminophenyl)imidazolidin-2-one

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Reagent Code: #129383
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CAS Number 938459-14-4

science Other reagents with same CAS 938459-14-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.2 g/mol
Formula C₉H₁₁N₃O
badge Registry Numbers
MDL Number MFCD09055391
inventory_2 Storage & Handling
Density 1.276±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system disorders. It serves as a building block in the preparation of compounds with potential anxiolytic and anticonvulsant properties. Also employed in research settings for the design of novel heterocyclic compounds in medicinal chemistry. Its amine and urea functionalities make it suitable for coupling reactions in organic synthesis, especially in the formation of more complex drug-like molecules.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,140.00
inventory 1g
10-20 days ฿19,790.00
1-(3-Aminophenyl)imidazolidin-2-one
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Used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system disorders. It serves as a building block in the preparation of compounds with potential anxiolytic and anticonvulsant properties. Also employed in research settings for the design of novel heterocyclic compounds in medicinal chemistry. Its amine and urea functionalities make it suitable for coupling reactions in organic synthesis, especially in the

Used in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for central nervous system disorders. It serves as a building block in the preparation of compounds with potential anxiolytic and anticonvulsant properties. Also employed in research settings for the design of novel heterocyclic compounds in medicinal chemistry. Its amine and urea functionalities make it suitable for coupling reactions in organic synthesis, especially in the formation of more complex drug-like molecules.

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