(R)-1-(2-(Trifluoromethyl)Phenyl)Ethanol

98%

Reagent Code: #231677
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CAS Number 127852-29-3

science Other reagents with same CAS 127852-29-3

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Weight 190.16 g/mol
Formula C₉H₉F₃O
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Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure, featuring a trifluoromethyl group adjacent to a chiral alcohol, makes it valuable in optimizing metabolic stability and binding affinity in drug candidates. Commonly employed in the production of central nervous system agents, anti-inflammatory compounds, and agrochemicals requiring high enantiomeric purity. Also utilized in asymmetric synthesis and catalysis research due to its ability to induce stereoselectivity in complex transformations.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,940.00
inventory 250mg
10-20 days ฿12,800.00
inventory 1g
10-20 days ฿25,580.00

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(R)-1-(2-(Trifluoromethyl)Phenyl)Ethanol
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Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure, featuring a trifluoromethyl group adjacent to a chiral alcohol, makes it valuable in optimizing metabolic stability and binding affinity in drug candidates. Commonly employed in the production of central nervous system agents, anti-inflammatory compounds, and agrochemicals requiring

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where stereochemistry plays a critical role in biological activity. Its structure, featuring a trifluoromethyl group adjacent to a chiral alcohol, makes it valuable in optimizing metabolic stability and binding affinity in drug candidates. Commonly employed in the production of central nervous system agents, anti-inflammatory compounds, and agrochemicals requiring high enantiomeric purity. Also utilized in asymmetric synthesis and catalysis research due to its ability to induce stereoselectivity in complex transformations.

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