Diethyl (2-(dimethylamino)-2-oxoethyl)phosphonate

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Reagent Code: #178611
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CAS Number 3842-86-2

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Weight 223.21 g/mol
Formula C₈H₁₈NO₄P
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of biologically active molecules and pharmaceuticals. Its phosphonate group enables Horner-Wadsworth-Emmons reactions, facilitating the formation of carbon-carbon double bonds, especially in the synthesis of alkenes with defined stereochemistry. Commonly applied in the development of antiviral and anticancer agents due to its ability to mimic phosphate esters in metabolic pathways. Also utilized in agrochemical synthesis for creating novel herbicides and plant growth regulators. Its dimethylamino group enhances solubility and reactivity, making it valuable in catalysis and ligand design.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,200.00
inventory 25g
10-20 days ฿8,000.00
inventory 100g
10-20 days ฿23,190.00
inventory 500g
10-20 days ฿96,000.00

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Diethyl (2-(dimethylamino)-2-oxoethyl)phosphonate
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Used as a key intermediate in organic synthesis, particularly in the preparation of biologically active molecules and pharmaceuticals. Its phosphonate group enables Horner-Wadsworth-Emmons reactions, facilitating the formation of carbon-carbon double bonds, especially in the synthesis of alkenes with defined stereochemistry. Commonly applied in the development of antiviral and anticancer agents due to its ability to mimic phosphate esters in metabolic pathways. Also utilized in agrochemical synthesis for

Used as a key intermediate in organic synthesis, particularly in the preparation of biologically active molecules and pharmaceuticals. Its phosphonate group enables Horner-Wadsworth-Emmons reactions, facilitating the formation of carbon-carbon double bonds, especially in the synthesis of alkenes with defined stereochemistry. Commonly applied in the development of antiviral and anticancer agents due to its ability to mimic phosphate esters in metabolic pathways. Also utilized in agrochemical synthesis for creating novel herbicides and plant growth regulators. Its dimethylamino group enhances solubility and reactivity, making it valuable in catalysis and ligand design.

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