Sodium 2,3,4,5,6-pentafluorobenzoate

95%

Reagent Code: #236031
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CAS Number 4830-57-3

science Other reagents with same CAS 4830-57-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.06 g/mol
Formula C₇F₅NaO₂
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MDL Number MFCD01652013
inventory_2 Storage & Handling
Storage Room temperature, inert gas storage

description Product Description

Used as a fluorinated building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its perfluorinated aromatic ring enhances lipophilicity and metabolic stability in target molecules, making it valuable in the development of bioactive compounds. Commonly employed in nucleophilic aromatic substitution reactions due to the electron-withdrawing effect of fluorine atoms. Also utilized in materials science for designing specialty polymers and liquid crystals with improved thermal and chemical resistance. Serves as a model compound in mechanistic studies involving fluorinated aromatics.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿320.00
inventory 5g
10-20 days ฿560.00
inventory 25g
10-20 days ฿2,590.00
inventory 100g
10-20 days ฿9,730.00
Sodium 2,3,4,5,6-pentafluorobenzoate
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Used as a fluorinated building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its perfluorinated aromatic ring enhances lipophilicity and metabolic stability in target molecules, making it valuable in the development of bioactive compounds. Commonly employed in nucleophilic aromatic substitution reactions due to the electron-withdrawing effect of fluorine atoms. Also utilized in materials science for designing specialty polymers and liquid crystals with improved the

Used as a fluorinated building block in organic synthesis, particularly in pharmaceutical and agrochemical research. Its perfluorinated aromatic ring enhances lipophilicity and metabolic stability in target molecules, making it valuable in the development of bioactive compounds. Commonly employed in nucleophilic aromatic substitution reactions due to the electron-withdrawing effect of fluorine atoms. Also utilized in materials science for designing specialty polymers and liquid crystals with improved thermal and chemical resistance. Serves as a model compound in mechanistic studies involving fluorinated aromatics.

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