3-[3-(trifluoromethyl)phenyl]prop-2-en-1-ol

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Reagent Code: #242449
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CAS Number 64189-17-9

science Other reagents with same CAS 64189-17-9

blur_circular Chemical Specifications

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Weight 202.17 g/mol
Formula C₁₀H₉OF₃
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Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of both the hydroxyl group and the trifluoromethyl-substituted aromatic system. The compound's structure allows for further functionalization, making it valuable in medicinal chemistry for building more complex molecules. It is also employed in the preparation of fluorinated analogs of natural products, where the trifluoromethyl group enhances metabolic stability and lipophilicity. Additionally, it finds use in the research of novel organic materials and as a building block in Suzuki and Heck coupling reactions for creating extended conjugated systems.

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inventory 10mg
10-20 days ฿3,380.00

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3-[3-(trifluoromethyl)phenyl]prop-2-en-1-ol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of both the hydroxyl group and the trifluoromethyl-substituted aromatic system. The compound's structure allows for further functionalization, making it valuable in medicinal chemistry for building more complex molecules. It is also employed in the preparation of fluorinated analogs of natural products, where the trifluoromethyl group enhances metabolic

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of bioactive molecules due to the presence of both the hydroxyl group and the trifluoromethyl-substituted aromatic system. The compound's structure allows for further functionalization, making it valuable in medicinal chemistry for building more complex molecules. It is also employed in the preparation of fluorinated analogs of natural products, where the trifluoromethyl group enhances metabolic stability and lipophilicity. Additionally, it finds use in the research of novel organic materials and as a building block in Suzuki and Heck coupling reactions for creating extended conjugated systems.

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