Diethyl 3-Bromobenzylphosphonate

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Reagent Code: #176572
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CAS Number 128833-03-4

science Other reagents with same CAS 128833-03-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 307.1207 g/mol
Formula C₁₁H₁₆BrO₃P
badge Registry Numbers
MDL Number MFCD07772009
thermostat Physical Properties
Boiling Point 310 ℃
inventory_2 Storage & Handling
Density 1.366 g/cm3
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of phosphonate-based compounds that serve as analogs of phosphate esters in medicinal chemistry. It plays a role in the development of pharmaceuticals, including antiviral and anticancer agents, due to its ability to participate in Horner-Wadsworth-Emmons reactions for forming carbon-carbon bonds. Also utilized in the synthesis of bioactive molecules and enzyme inhibitors where the phosphonate group mimics natural phosphate intermediates. Its bromo substituent allows for further functionalization via cross-coupling reactions, making it a versatile building block in drug discovery and agrochemical research.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿1,150.00
inventory 25g
10-20 days ฿5,200.00
inventory 100g
10-20 days ฿15,780.00

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Diethyl 3-Bromobenzylphosphonate
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Used as an intermediate in organic synthesis, particularly in the preparation of phosphonate-based compounds that serve as analogs of phosphate esters in medicinal chemistry. It plays a role in the development of pharmaceuticals, including antiviral and anticancer agents, due to its ability to participate in Horner-Wadsworth-Emmons reactions for forming carbon-carbon bonds. Also utilized in the synthesis of bioactive molecules and enzyme inhibitors where the phosphonate group mimics natural phosphate int

Used as an intermediate in organic synthesis, particularly in the preparation of phosphonate-based compounds that serve as analogs of phosphate esters in medicinal chemistry. It plays a role in the development of pharmaceuticals, including antiviral and anticancer agents, due to its ability to participate in Horner-Wadsworth-Emmons reactions for forming carbon-carbon bonds. Also utilized in the synthesis of bioactive molecules and enzyme inhibitors where the phosphonate group mimics natural phosphate intermediates. Its bromo substituent allows for further functionalization via cross-coupling reactions, making it a versatile building block in drug discovery and agrochemical research.

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