3-(Trifluoromethyl)mandelic Acid

≥95%

Reagent Code: #244925
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CAS Number 349-10-0

science Other reagents with same CAS 349-10-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.15 g/mol
Formula C₉H₇F₃O₃
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MDL Number MFCD00014339
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improved bioavailability and binding affinity. Commonly employed in asymmetric synthesis and catalysis, it serves as a precursor for anticoagulants, antiviral agents, and central nervous system drugs. Also utilized in the preparation of chiral ligands and organocatalysts for stereoselective transformations.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿41,510.00
3-(Trifluoromethyl)mandelic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improved bioavailability and binding affinity. Commonly employed in asymmetric synthesis and catalysis, it serves as a precursor for anticoagulants, antiviral agents, and central nervous system drugs. Also utilized i

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design for improved bioavailability and binding affinity. Commonly employed in asymmetric synthesis and catalysis, it serves as a precursor for anticoagulants, antiviral agents, and central nervous system drugs. Also utilized in the preparation of chiral ligands and organocatalysts for stereoselective transformations.

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