3-(5-Bromo-2-fluorophenyl)propan-1-ol

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Reagent Code: #117475
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CAS Number 1057673-68-3

science Other reagents with same CAS 1057673-68-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.08 g/mol
Formula C₉H₁₀BrFO
badge Registry Numbers
MDL Number MFCD09028747
thermostat Physical Properties
Boiling Point 295.2±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.487±0.06 g/cm3(Predicted)
Storage Room temperature, dark, inert gas

description Product Description

This compound is primarily used in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both a bromo and a fluoro substituent on the phenyl ring, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The bromine atom can facilitate further functionalization through cross-coupling reactions, while the fluorine atom often enhances the biological activity and metabolic stability of the final product. Additionally, the propanol side chain provides a versatile handle for further chemical modifications, enabling the creation of a wide range of derivatives with potential applications in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,883.00
inventory 250mg
10-20 days ฿15,975.00
inventory 1g
10-20 days ฿44,730.00

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3-(5-Bromo-2-fluorophenyl)propan-1-ol
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This compound is primarily used in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both a bromo and a fluoro substituent on the phenyl ring, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The bromine atom can facilitate further functionalization through cross-coupling reactions, while the fluorine atom often enhances the biological activity and metabolic stability of the fi

This compound is primarily used in the field of organic synthesis, where it serves as a key intermediate in the production of more complex molecules. Its structure, featuring both a bromo and a fluoro substituent on the phenyl ring, makes it particularly valuable in the development of pharmaceuticals and agrochemicals. The bromine atom can facilitate further functionalization through cross-coupling reactions, while the fluorine atom often enhances the biological activity and metabolic stability of the final product. Additionally, the propanol side chain provides a versatile handle for further chemical modifications, enabling the creation of a wide range of derivatives with potential applications in drug discovery and material science.

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