3-(2,5-difluorophenyl)prop-2-yn-1-ol

95%

Reagent Code: #85272
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CAS Number 109034-27-7

science Other reagents with same CAS 109034-27-7

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Weight 168.14 g/mol
Formula C₉H₆F₂O
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MDL Number MFCD06803808
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This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a difluorophenyl group and a propargylic alcohol moiety, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. It is often employed in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), to generate triazole derivatives, which are widely explored for their medicinal properties. Additionally, it serves as a building block in the preparation of agrochemicals and specialty chemicals, where the fluorine atoms enhance stability and bioavailability. Its application extends to materials science, where it is used in the development of advanced polymers and coatings with tailored properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,020.00
inventory 250mg
10-20 days ฿12,870.00
inventory 1g
10-20 days ฿25,740.00

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3-(2,5-difluorophenyl)prop-2-yn-1-ol
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This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a difluorophenyl group and a propargylic alcohol moiety, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. It is often employed in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), to generate triazole derivatives, which are widely e

This chemical is primarily utilized in organic synthesis as a key intermediate for the development of more complex molecules. Its structure, featuring a difluorophenyl group and a propargylic alcohol moiety, makes it valuable in the construction of pharmaceuticals, particularly in the synthesis of compounds with potential biological activity. It is often employed in click chemistry reactions, such as copper-catalyzed azide-alkyne cycloaddition (CuAAC), to generate triazole derivatives, which are widely explored for their medicinal properties. Additionally, it serves as a building block in the preparation of agrochemicals and specialty chemicals, where the fluorine atoms enhance stability and bioavailability. Its application extends to materials science, where it is used in the development of advanced polymers and coatings with tailored properties.

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