Ethyl 2-((4-methoxyphenyl)amino)-2-oxoacetate

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Reagent Code: #184414
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CAS Number 18522-99-1

science Other reagents with same CAS 18522-99-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 223.23 g/mol
Formula C₁₁H₁₃NO₄
badge Registry Numbers
MDL Number MFCD00157580
thermostat Physical Properties
Melting Point 245 °C
inventory_2 Storage & Handling
Density 1.219±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for constructing heterocyclic compounds, including certain kinase inhibitors and antimicrobial agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing bioactive molecules. Commonly employed in condensation reactions to form more complex esters and amides with potential therapeutic activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿950.00
inventory 1g
10-20 days ฿2,540.00
inventory 5g
10-20 days ฿8,900.00

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Ethyl 2-((4-methoxyphenyl)amino)-2-oxoacetate
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for constructing heterocyclic compounds, including certain kinase inhibitors and antimicrobial agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing bioactive molecules. Commonly employed in condensation reactions to form more complex esters and amides with potential therapeutic activity.

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. It serves as a building block for constructing heterocyclic compounds, including certain kinase inhibitors and antimicrobial agents. Its structure allows for easy functionalization, making it valuable in medicinal chemistry for developing bioactive molecules. Commonly employed in condensation reactions to form more complex esters and amides with potential therapeutic activity.

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