(E)-Methyl 2-(((2,2-dimethoxyethyl)amino)methylene)-4-methoxy-3-oxobutanoate

95%

Reagent Code: #181110
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CAS Number 1646862-12-5

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 261.27 g/mol
Formula C₁₁H₁₉NO₆
badge Registry Numbers
MDL Number MFCD32671509
thermostat Physical Properties
Boiling Point 339.0±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.124±0.06 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor and antimicrobial properties. Its structure allows for easy modification in multistep organic reactions, making it valuable in medicinal chemistry research. Commonly employed in the preparation of heterocyclic compounds due to its reactive enamine and ester functionalities. Also utilized in the design of kinase inhibitors and other enzyme-targeted drugs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,220.00
inventory 5g
10-20 days ฿4,600.00

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(E)-Methyl 2-(((2,2-dimethoxyethyl)amino)methylene)-4-methoxy-3-oxobutanoate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor and antimicrobial properties. Its structure allows for easy modification in multistep organic reactions, making it valuable in medicinal chemistry research. Commonly employed in the preparation of heterocyclic compounds due to its reactive enamine and ester functionalities. Also utilized in the design of kinase inhibitors and other enzyme-targeted drugs.

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules with potential antitumor and antimicrobial properties. Its structure allows for easy modification in multistep organic reactions, making it valuable in medicinal chemistry research. Commonly employed in the preparation of heterocyclic compounds due to its reactive enamine and ester functionalities. Also utilized in the design of kinase inhibitors and other enzyme-targeted drugs.

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