ethyl 3-dimethoxyphosphorylpropanoate

95%

Reagent Code: #184555
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CAS Number 23550-25-6

science Other reagents with same CAS 23550-25-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.16 g/mol
Formula C₇H₁₅O₅P
badge Registry Numbers
MDL Number MFCD00775368
thermostat Physical Properties
Boiling Point 278.8±23.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.139±0.06 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of biologically active compounds containing phosphonate groups. Its structure allows for the introduction of phosphonate moieties into organic frameworks, making it valuable in medicinal chemistry for developing enzyme inhibitors and antiviral agents. Commonly employed in Horner-Wadsworth-Emmons reactions to form carbon-carbon bonds, especially in the construction of conjugated systems like alkenes. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the stability and reactivity of the phosphonate functionality. Suitable for lab-scale synthesis and optimization of phosphorylated molecules.

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inventory 1g
10-20 days ฿32,720.00

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ethyl 3-dimethoxyphosphorylpropanoate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of biologically active compounds containing phosphonate groups. Its structure allows for the introduction of phosphonate moieties into organic frameworks, making it valuable in medicinal chemistry for developing enzyme inhibitors and antiviral agents. Commonly employed in Horner-Wadsworth-Emmons reactions to form carbon-carbon bonds, especially in the construction of conjugated systems like alkenes. Also utili

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the preparation of biologically active compounds containing phosphonate groups. Its structure allows for the introduction of phosphonate moieties into organic frameworks, making it valuable in medicinal chemistry for developing enzyme inhibitors and antiviral agents. Commonly employed in Horner-Wadsworth-Emmons reactions to form carbon-carbon bonds, especially in the construction of conjugated systems like alkenes. Also utilized in agrochemical research for designing novel pesticides and herbicides due to the stability and reactivity of the phosphonate functionality. Suitable for lab-scale synthesis and optimization of phosphorylated molecules.

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