3-(Trifluoromethyl)propiophenone

>97.0%(GC)

Reagent Code: #240032
label
Alias 3'-(trifluoromethyl)phenylacetone; 3-(trifluoromethyl)phenylacetone
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CAS Number 1533-03-5

science Other reagents with same CAS 1533-03-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 202.17 g/mol
Formula C₁₀H₉F₃O
badge Registry Numbers
MDL Number MFCD00039227
thermostat Physical Properties
Melting Point 18 °C
Boiling Point 216-217 °C(lit.)
inventory_2 Storage & Handling
Density 1.202 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for the introduction of trifluoromethyl groups into more complex molecules, which can enhance metabolic stability and bioavailability in drug design. Commonly employed in the development of anti-inflammatory agents, antidepressants, and antipsychotic compounds. Also utilized in the preparation of specialty chemicals where fluorinated moieties improve performance, such as in certain herbicides and fungicides. Its reactivity makes it valuable in organic transformations, particularly in carbon-carbon bond formation and nucleophilic addition reactions.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿148.50
inventory 5g
10-20 days ฿350.00
inventory 25g
10-20 days ฿946.00

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3-(Trifluoromethyl)propiophenone
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Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for the introduction of trifluoromethyl groups into more complex molecules, which can enhance metabolic stability and bioavailability in drug design. Commonly employed in the development of anti-inflammatory agents, antidepressants, and antipsychotic compounds. Also utilized in the preparation of specialty chemicals where fluorinated moieties improve performance, such as in certain herbicides and

Used primarily as an intermediate in the synthesis of pharmaceuticals and agrochemicals. Its structure allows for the introduction of trifluoromethyl groups into more complex molecules, which can enhance metabolic stability and bioavailability in drug design. Commonly employed in the development of anti-inflammatory agents, antidepressants, and antipsychotic compounds. Also utilized in the preparation of specialty chemicals where fluorinated moieties improve performance, such as in certain herbicides and fungicides. Its reactivity makes it valuable in organic transformations, particularly in carbon-carbon bond formation and nucleophilic addition reactions.

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