Phenethyl 2,2,2-trifluoroacetate

95%

Reagent Code: #223064
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CAS Number 55419-66-4

science Other reagents with same CAS 55419-66-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.17 g/mol
Formula C₁₀H₉F₃O₂
badge Registry Numbers
MDL Number MFCD00755553
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its trifluoroacetate group facilitates easy deprotection under mild conditions, making it valuable in multi-step synthesis where selective reaction control is needed. The phenethyl moiety can act as a protecting group for carboxylic acids or be incorporated into bioactive molecules. It is also employed in the preparation of fluorinated compounds, taking advantage of the electron-withdrawing properties of the trifluoromethyl group to modulate reactivity or enhance metabolic stability in drug candidates.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿8,010.00
1g
10-20 days ฿21,600.00
5g
10-20 days ฿75,600.00
Phenethyl 2,2,2-trifluoroacetate
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Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its trifluoroacetate group facilitates easy deprotection under mild conditions, making it valuable in multi-step synthesis where selective reaction control is needed. The phenethyl moiety can act as a protecting group for carboxylic acids or be incorporated into bioactive molecules. It is also employed in the preparation of fluorinated compounds, taking advantage of the electron-withdrawing propertie

Used as an intermediate in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its trifluoroacetate group facilitates easy deprotection under mild conditions, making it valuable in multi-step synthesis where selective reaction control is needed. The phenethyl moiety can act as a protecting group for carboxylic acids or be incorporated into bioactive molecules. It is also employed in the preparation of fluorinated compounds, taking advantage of the electron-withdrawing properties of the trifluoromethyl group to modulate reactivity or enhance metabolic stability in drug candidates.

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