2,2,2-Trifluoroethyl 2-bromoacetate

95%

Reagent Code: #238326
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CAS Number 61433-91-8

science Other reagents with same CAS 61433-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.97 g/mol
Formula C₄H₄BrF₃O₂
badge Registry Numbers
MDL Number MFCD18975644
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a specialty intermediate in organic synthesis, this compound serves in the preparation of fluorinated pharmaceuticals and agrochemicals. The presence of both a bromoacetate group and a trifluoroethyl moiety makes it valuable for introducing fluorinated segments into larger molecules, enhancing metabolic stability and lipophilicity. It is commonly employed in alkylation reactions and as a building block in the development of bioactive compounds, particularly in medicinal chemistry research. Its reactivity allows for selective transformations under controlled conditions, making it suitable for use in multi-step synthetic routes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,550.00
inventory 250mg
10-20 days ฿17,930.00
inventory 1g
10-20 days ฿48,400.00

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2,2,2-Trifluoroethyl 2-bromoacetate
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Used primarily as a specialty intermediate in organic synthesis, this compound serves in the preparation of fluorinated pharmaceuticals and agrochemicals. The presence of both a bromoacetate group and a trifluoroethyl moiety makes it valuable for introducing fluorinated segments into larger molecules, enhancing metabolic stability and lipophilicity. It is commonly employed in alkylation reactions and as a building block in the development of bioactive compounds, particularly in medicinal chemistry resear

Used primarily as a specialty intermediate in organic synthesis, this compound serves in the preparation of fluorinated pharmaceuticals and agrochemicals. The presence of both a bromoacetate group and a trifluoroethyl moiety makes it valuable for introducing fluorinated segments into larger molecules, enhancing metabolic stability and lipophilicity. It is commonly employed in alkylation reactions and as a building block in the development of bioactive compounds, particularly in medicinal chemistry research. Its reactivity allows for selective transformations under controlled conditions, making it suitable for use in multi-step synthetic routes.

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