(S)-3-AMINO-4-(2,4,5-TRIFLUORO-PHENYL)-BUTYRIC ACID-HCL

98%

Reagent Code: #96573
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CAS Number 1217809-78-3

science Other reagents with same CAS 1217809-78-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 269.65 g/mol
Formula C₁₀H₁₁ClF₃NO₂
badge Registry Numbers
MDL Number MFCD06659149
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, such as epilepsy and Parkinson’s disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a neurotransmitter. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, contributing to advancements in the treatment of metabolic and psychiatric conditions. Its trifluorophenyl group enhances binding affinity and stability, making it valuable in drug design and optimization.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿3,627.00
inventory 250mg
10-20 days ฿10,251.00
inventory 1g
10-20 days ฿30,537.00

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(S)-3-AMINO-4-(2,4,5-TRIFLUORO-PHENYL)-BUTYRIC ACID-HCL
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This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, such as epilepsy and Parkinson’s disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a neurotransmitter. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, contributing to advancements in the t

This compound is primarily utilized in pharmaceutical research and development, particularly in the synthesis of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs targeting neurological disorders, such as epilepsy and Parkinson’s disease, due to its structural similarity to gamma-aminobutyric acid (GABA), a neurotransmitter. Additionally, it is employed in the development of enzyme inhibitors and receptor modulators, contributing to advancements in the treatment of metabolic and psychiatric conditions. Its trifluorophenyl group enhances binding affinity and stability, making it valuable in drug design and optimization.

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