Diethyl 2,2,3,3-Tetrafluorosuccinate

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Reagent Code: #178855
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CAS Number 377-71-9

science Other reagents with same CAS 377-71-9

blur_circular Chemical Specifications

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Weight 246.16 g/mol
Formula C₈H₁₀F₄O₄
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MDL Number MFCD00015155
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a fluorinated building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its ester groups and fluorinated backbone make it suitable for constructing complex molecules with enhanced metabolic stability and bioavailability. Commonly employed in the preparation of fluorinated analogs of biologically active compounds, where the presence of fluorine atoms can improve lipophilicity and binding affinity. Also utilized in materials science for developing specialty polymers with unique thermal and chemical resistance properties. The compound’s reactivity allows for selective transformations, enabling the introduction of fluorinated segments into larger molecular frameworks.

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inventory 250mg
10-20 days ฿560.00

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Diethyl 2,2,3,3-Tetrafluorosuccinate
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Used as a fluorinated building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its ester groups and fluorinated backbone make it suitable for constructing complex molecules with enhanced metabolic stability and bioavailability. Commonly employed in the preparation of fluorinated analogs of biologically active compounds, where the presence of fluorine atoms can improve lipophilicity and binding affinity. Also utilized in materials science for developing specialty po

Used as a fluorinated building block in organic synthesis, particularly in pharmaceutical and agrochemical industries. Its ester groups and fluorinated backbone make it suitable for constructing complex molecules with enhanced metabolic stability and bioavailability. Commonly employed in the preparation of fluorinated analogs of biologically active compounds, where the presence of fluorine atoms can improve lipophilicity and binding affinity. Also utilized in materials science for developing specialty polymers with unique thermal and chemical resistance properties. The compound’s reactivity allows for selective transformations, enabling the introduction of fluorinated segments into larger molecular frameworks.

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