3-Bromo-4-(trifluoromethoxy)phenol

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Reagent Code: #152260
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CAS Number 886496-88-4

science Other reagents with same CAS 886496-88-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.01 g/mol
Formula C₇H₄BrF₃O₂
badge Registry Numbers
MDL Number MFCD05864310
thermostat Physical Properties
Boiling Point 233.5±35.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.779±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof, inert gas

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require halogenated aromatic scaffolds. Its structure supports the creation of more complex compounds with enhanced metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and inflammatory conditions. Also utilized in the preparation of fluorinated analogs to improve lipophilicity and bioavailability in lead compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,280.00
inventory 1g
10-20 days ฿3,200.00
inventory 5g
10-20 days ฿12,800.00

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3-Bromo-4-(trifluoromethoxy)phenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require halogenated aromatic scaffolds. Its structure supports the creation of more complex compounds with enhanced metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and inflammatory conditions. Also utilized in the preparation of fluorinated analogs to improve

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules that require halogenated aromatic scaffolds. Its structure supports the creation of more complex compounds with enhanced metabolic stability and binding affinity. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders and inflammatory conditions. Also utilized in the preparation of fluorinated analogs to improve lipophilicity and bioavailability in lead compounds.

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