4-Bromobenzylphosphonic acid

97%

Reagent Code: #129408
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CAS Number 40962-34-3

science Other reagents with same CAS 40962-34-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.01 g/mol
Formula C₇H₈BrO₃P
badge Registry Numbers
MDL Number MFCD03411189
thermostat Physical Properties
Melting Point 189-193 °C
Boiling Point 438.6±47.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.779±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other bioactive molecules. Its phosphonic acid group allows it to mimic phosphate esters in biological systems, making it valuable in the design of enzyme inhibitors. Also employed in materials science for surface modification of metal oxides and in the preparation of functionalized polymers. Its bromo substituent enables further functionalization via cross-coupling reactions, enhancing its utility in organic synthesis.

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inventory 1g
10-20 days ฿6,420.00

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4-Bromobenzylphosphonic acid
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other bioactive molecules. Its phosphonic acid group allows it to mimic phosphate esters in biological systems, making it valuable in the design of enzyme inhibitors. Also employed in materials science for surface modification of metal oxides and in the preparation of functionalized polymers. Its bromo substituent enables further functionalization via cross-coupling r

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of kinase inhibitors and other bioactive molecules. Its phosphonic acid group allows it to mimic phosphate esters in biological systems, making it valuable in the design of enzyme inhibitors. Also employed in materials science for surface modification of metal oxides and in the preparation of functionalized polymers. Its bromo substituent enables further functionalization via cross-coupling reactions, enhancing its utility in organic synthesis.

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