(S)-3,3,3-Trifluoro-2-hydroxy-2-methylpropionic Acid

97%

Reagent Code: #235169
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CAS Number 24435-45-8

science Other reagents with same CAS 24435-45-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.08 g/mol
Formula C₄H₅F₃O₃
badge Registry Numbers
MDL Number MFCD03092898
thermostat Physical Properties
Melting Point 110°C
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of fluorinated drugs where metabolic stability and bioavailability are enhanced by the trifluoromethyl group. Its hydroxyl and carboxylic acid functionalities allow for easy derivatization, making it valuable in asymmetric synthesis and the preparation of enzyme inhibitors. Commonly employed in the production of active pharmaceutical ingredients (APIs) that target central nervous system disorders and inflammatory diseases due to its ability to influence stereochemistry and improve pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,240.00
inventory 5g
10-20 days ฿6,150.00
(S)-3,3,3-Trifluoro-2-hydroxy-2-methylpropionic Acid
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Used as a chiral building block in pharmaceutical synthesis, particularly in the development of fluorinated drugs where metabolic stability and bioavailability are enhanced by the trifluoromethyl group. Its hydroxyl and carboxylic acid functionalities allow for easy derivatization, making it valuable in asymmetric synthesis and the preparation of enzyme inhibitors. Commonly employed in the production of active pharmaceutical ingredients (APIs) that target central nervous system disorders and inflammatory

Used as a chiral building block in pharmaceutical synthesis, particularly in the development of fluorinated drugs where metabolic stability and bioavailability are enhanced by the trifluoromethyl group. Its hydroxyl and carboxylic acid functionalities allow for easy derivatization, making it valuable in asymmetric synthesis and the preparation of enzyme inhibitors. Commonly employed in the production of active pharmaceutical ingredients (APIs) that target central nervous system disorders and inflammatory diseases due to its ability to influence stereochemistry and improve pharmacokinetic properties.

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