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Home  > 2-[3-(trifluoromethyl)pyrazol-1-yl]ethanol

AJ05514

1006344-06-4 | 2-[3-(trifluoromethyl)pyrazol-1-yl]ethanol

Packsize Purity Availability Price Discounted Price    Quantity
50mg 95% 1 week $296.00 $207.00 -   +
100mg 95% 1 week $400.00 $280.00 -   +
250mg 95% 1 week $538.00 $376.00 -   +
500mg 95% 1 week $799.00 $559.00 -   +
1g 95% 1 week $1,002.00 $701.00 -   +

*All products are for research use only and not intended for human or animal use.

*All prices are in USD.

Description
Catalog Number: AJ05514
Chemical Name: 2-[3-(trifluoromethyl)pyrazol-1-yl]ethanol
CAS Number: 1006344-06-4
Molecular Formula: C6H7F3N2O
Molecular Weight: 180.1278
MDL Number: MFCD06804923
SMILES: OCCn1ccc(n1)C(F)(F)F

 

Upstream Synthesis Route
  • The compound 2-[3-(Trifluoromethyl)-1H-pyrazol-1-yl]ethan-1-ol, commonly referred to as $name$, plays a significant role in chemical synthesis as a versatile building block. Its unique structure, featuring a trifluoromethyl group attached to a pyrazole ring, imparts valuable properties that are beneficial in various synthetic pathways. $name$ is frequently utilized as a key intermediate in the synthesis of pharmaceuticals, agrochemicals, and other fine chemicals. The presence of the trifluoromethyl group enhances the compound's lipophilicity and electron-withdrawing nature, making it a valuable component in medicinal chemistry for drug design. Additionally, the pyrazole ring confers reactivity that enables diverse functionalization and manipulation during chemical transformations.In organic synthesis, $name$ can serve as a starting material for the construction of complex molecular structures through functional group interconversions, such as oxidation, reduction, or substitution reactions. Its ability to participate in various chemical reactions makes it a valuable tool for accessing a wide range of molecular architectures with specific properties.Furthermore, $name$ can also be employed in material science for the modification of polymers, surfaces, and other materials, where the trifluoromethyl group can impart enhanced hydrophobicity and chemical stability. Its versatility and reactivity make it a valuable asset in the toolkit of synthetic chemists for designing and accessing novel compounds with tailored properties for a variety of applications.
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