diethyl (2-chloro-6-fluorobenzyl)phosphonate

95%

Reagent Code: #87051
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CAS Number 680214-57-7

science Other reagents with same CAS 680214-57-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.66 g/mol
Formula C₁₁H₁₅ClFO₃P
badge Registry Numbers
MDL Number MFCD00125503
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various biologically active molecules. It is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where its phosphonate group enables the introduction of phosphorus-containing functionalities into target molecules. The presence of the chloro and fluoro substituents on the benzyl ring enhances its reactivity and selectivity in cross-coupling reactions, making it a useful building block for constructing complex aromatic systems. Additionally, it finds application in the development of herbicides and insecticides, contributing to improved crop protection strategies. Its stability and versatility make it a preferred choice in medicinal chemistry for designing novel drug candidates with potential therapeutic effects.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,671.00

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diethyl (2-chloro-6-fluorobenzyl)phosphonate
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This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various biologically active molecules. It is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where its phosphonate group enables the introduction of phosphorus-containing functionalities into target molecules. The presence of the chloro and fluoro substituents on the benzyl ring enhances its reactivity and selectivity in cross-coupling reactions, making it a useful building b

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of various biologically active molecules. It is particularly valuable in the synthesis of agrochemicals and pharmaceuticals, where its phosphonate group enables the introduction of phosphorus-containing functionalities into target molecules. The presence of the chloro and fluoro substituents on the benzyl ring enhances its reactivity and selectivity in cross-coupling reactions, making it a useful building block for constructing complex aromatic systems. Additionally, it finds application in the development of herbicides and insecticides, contributing to improved crop protection strategies. Its stability and versatility make it a preferred choice in medicinal chemistry for designing novel drug candidates with potential therapeutic effects.

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