(S)-1-(3,5-Bis(trifluoromethyl)phenyl)ethanol

≥95%

Reagent Code: #234886
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CAS Number 225920-05-8

science Other reagents with same CAS 225920-05-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 258.16 g/mol
Formula C₁₀H₈F₆O
badge Registry Numbers
MDL Number MFCD03093011
thermostat Physical Properties
Boiling Point 223.5ºC at 760mmHg
inventory_2 Storage & Handling
Density 1.457g/ml
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where enantioselectivity is critical. Its structure supports the development of agents targeting central nervous system disorders and inflammatory conditions. The presence of trifluoromethyl groups enhances metabolic stability and lipophilicity, improving drug penetration across biological membranes. Commonly employed in asymmetric synthesis and catalysis to construct complex molecules with high optical purity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿168.00
inventory 5g
10-20 days ฿450.00
inventory 100g
10-20 days ฿8,010.00
inventory 25g
10-20 days ฿2,100.00
(S)-1-(3,5-Bis(trifluoromethyl)phenyl)ethanol
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where enantioselectivity is critical. Its structure supports the development of agents targeting central nervous system disorders and inflammatory conditions. The presence of trifluoromethyl groups enhances metabolic stability and lipophilicity, improving drug penetration across biological membranes. Commonly employed in asymmetric synthesis and catalysis to construct complex molecules with hi

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals where enantioselectivity is critical. Its structure supports the development of agents targeting central nervous system disorders and inflammatory conditions. The presence of trifluoromethyl groups enhances metabolic stability and lipophilicity, improving drug penetration across biological membranes. Commonly employed in asymmetric synthesis and catalysis to construct complex molecules with high optical purity.

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