N-[(2,3,4,5,6-pentafluorophenyl)methylidene]hydroxylamine

95%

Reagent Code: #216013
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CAS Number 27318-28-1

science Other reagents with same CAS 27318-28-1

blur_circular Chemical Specifications

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Weight 211.09 g/mol
Formula C₇H₂F₅NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily as a reactive intermediate in organic synthesis, especially in the preparation of fluorinated compounds for pharmaceuticals and agrochemicals. Its unique pentafluorophenyl group enhances electron-withdrawing properties, making it valuable in cycloaddition reactions and as a building block in the development of functional materials. It also serves as a precursor in the synthesis of isonitriles and other nitrogen-containing heterocycles, which are important in medicinal chemistry. Due to its stability imparted by fluorine substitution, it is favored in reactions requiring selective transformations under mild conditions.

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inventory 1g
10-20 days ฿14,250.00

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N-[(2,3,4,5,6-pentafluorophenyl)methylidene]hydroxylamine
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Used primarily as a reactive intermediate in organic synthesis, especially in the preparation of fluorinated compounds for pharmaceuticals and agrochemicals. Its unique pentafluorophenyl group enhances electron-withdrawing properties, making it valuable in cycloaddition reactions and as a building block in the development of functional materials. It also serves as a precursor in the synthesis of isonitriles and other nitrogen-containing heterocycles, which are important in medicinal chemistry. Due to its

Used primarily as a reactive intermediate in organic synthesis, especially in the preparation of fluorinated compounds for pharmaceuticals and agrochemicals. Its unique pentafluorophenyl group enhances electron-withdrawing properties, making it valuable in cycloaddition reactions and as a building block in the development of functional materials. It also serves as a precursor in the synthesis of isonitriles and other nitrogen-containing heterocycles, which are important in medicinal chemistry. Due to its stability imparted by fluorine substitution, it is favored in reactions requiring selective transformations under mild conditions.

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