(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride

≥95%

Reagent Code: #38263
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CAS Number 921609-34-9

science Other reagents with same CAS 921609-34-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.65 g/mol
Formula C₁₀H₁₁ClF₃NO₃
badge Registry Numbers
MDL Number MFCD28986154
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological disorders. Its structure, featuring a trifluoromethoxy group, enhances its potential in developing drugs with improved metabolic stability and bioavailability. Researchers often employ it in the design of compounds that interact with specific receptors or enzymes in the central nervous system, making it valuable for studying conditions like epilepsy, depression, and chronic pain. Additionally, its chiral nature allows for the exploration of enantioselective interactions in drug development, contributing to the creation of more effective and targeted therapies.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,013.00
inventory 100mg
10-20 days ฿2,763.00

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(S)-2-Amino-3-(4-(trifluoromethoxy)phenyl)propanoic acid hydrochloride
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This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological disorders. Its structure, featuring a trifluoromethoxy group, enhances its potential in developing drugs with improved metabolic stability and bioavailability. Researchers often employ it in the design of compounds that interact with specific receptors or enzymes in the cent

This compound is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological disorders. Its structure, featuring a trifluoromethoxy group, enhances its potential in developing drugs with improved metabolic stability and bioavailability. Researchers often employ it in the design of compounds that interact with specific receptors or enzymes in the central nervous system, making it valuable for studying conditions like epilepsy, depression, and chronic pain. Additionally, its chiral nature allows for the exploration of enantioselective interactions in drug development, contributing to the creation of more effective and targeted therapies.

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