(R)-3,3,3-Trifluoro-2-hydroxy-2-methylpropionic acid

98%

Reagent Code: #229973
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CAS Number 44864-47-3

science Other reagents with same CAS 44864-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.08 g/mol
Formula C₄H₅F₃O₃
badge Registry Numbers
MDL Number MFCD03095400
thermostat Physical Properties
Melting Point 110 °C
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design. The hydroxyl and carboxylic acid functionalities allow for further chemical modifications, enabling its incorporation into complex organic structures. Commonly employed in asymmetric synthesis due to its stereochemical purity, it helps control the three-dimensional configuration of target compounds, which is critical for biological activity in medicinal chemistry.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿910.00
inventory 25g
10-20 days ฿14,200.00
inventory 100g
10-20 days ฿55,560.00
inventory 5g
10-20 days ฿2,880.00

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(R)-3,3,3-Trifluoro-2-hydroxy-2-methylpropionic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design. The hydroxyl and carboxylic acid functionalities allow for further chemical modifications, enabling its incorporation into complex organic structures. Commonly employed in asymmetric synthesis due to its stereochemical purity, it helps control the three

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its trifluoromethyl group enhances metabolic stability and lipophilicity, making it valuable in drug design. The hydroxyl and carboxylic acid functionalities allow for further chemical modifications, enabling its incorporation into complex organic structures. Commonly employed in asymmetric synthesis due to its stereochemical purity, it helps control the three-dimensional configuration of target compounds, which is critical for biological activity in medicinal chemistry.

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