4-Iodo-3-(trifluoromethyl)benzoic acid

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Reagent Code: #79524
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CAS Number 914636-20-7

science Other reagents with same CAS 914636-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 316.02 g/mol
Formula C₈H₄F₃IO₂
badge Registry Numbers
MDL Number MFCD09258947
thermostat Physical Properties
Boiling Point 311.7±42.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

Used in organic synthesis as a building block for creating more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the development of active pharmaceutical ingredients (APIs) and agrochemicals. Its trifluoromethyl group enhances the biological activity and metabolic stability of the compounds it helps form. Also employed in the preparation of ligands for catalysis and in materials science for designing advanced functional materials. Its iodine moiety makes it a useful precursor for cross-coupling reactions in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿468.00
inventory 250mg
10-20 days ฿702.00
inventory 1g
10-20 days ฿1,755.00
inventory 5g
10-20 days ฿5,607.00

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4-Iodo-3-(trifluoromethyl)benzoic acid
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Used in organic synthesis as a building block for creating more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the development of active pharmaceutical ingredients (APIs) and agrochemicals. Its trifluoromethyl group enhances the biological activity and metabolic stability of the compounds it helps form. Also employed in the preparation of ligands for catalysis and in materials science for designing advanced functional materials. Its iodine moiety makes it a us

Used in organic synthesis as a building block for creating more complex molecules, particularly in pharmaceutical research. It serves as an intermediate in the development of active pharmaceutical ingredients (APIs) and agrochemicals. Its trifluoromethyl group enhances the biological activity and metabolic stability of the compounds it helps form. Also employed in the preparation of ligands for catalysis and in materials science for designing advanced functional materials. Its iodine moiety makes it a useful precursor for cross-coupling reactions in medicinal chemistry.

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