2-TRIFLUOROMETHYL-2-PROPANOL

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Reagent Code: #240462
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CAS Number 507-52-8

science Other reagents with same CAS 507-52-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 128.09 g/mol
Formula C₄H₇F₃O
badge Registry Numbers
MDL Number MFCD00014391
thermostat Physical Properties
Boiling Point 83°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a solvent and intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its fluorinated structure enhances stability and lipophilicity, making it valuable in the development of active ingredients that require improved metabolic resistance. Also employed in specialty coatings and polymers where resistance to heat, chemicals, or UV degradation is needed. Shows utility in the preparation of fluorinated building blocks for medicinal chemistry due to the strong electron-withdrawing effect of the trifluoromethyl group.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿4,820.00

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2-TRIFLUOROMETHYL-2-PROPANOL
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Used as a solvent and intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its fluorinated structure enhances stability and lipophilicity, making it valuable in the development of active ingredients that require improved metabolic resistance. Also employed in specialty coatings and polymers where resistance to heat, chemicals, or UV degradation is needed. Shows utility in the preparation of fluorinated building blocks for medicinal chemistry due to the strong electron-wit

Used as a solvent and intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. Its fluorinated structure enhances stability and lipophilicity, making it valuable in the development of active ingredients that require improved metabolic resistance. Also employed in specialty coatings and polymers where resistance to heat, chemicals, or UV degradation is needed. Shows utility in the preparation of fluorinated building blocks for medicinal chemistry due to the strong electron-withdrawing effect of the trifluoromethyl group.

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