(S)-3-((tert-Butoxycarbonyl)amino)-3-(3-(trifluoromethyl)phenyl)propanoic acid

95%

Reagent Code: #235984
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CAS Number 500770-78-5

science Other reagents with same CAS 500770-78-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 333.3 g/mol
Formula C₁₅H₁₈F₃NO₄
badge Registry Numbers
MDL Number MFCD03427926
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and antidepressants. Its structure supports the development of selective serotonin reuptake inhibitors (SSRIs) due to the presence of the trifluoromethylphenyl group, which enhances metabolic stability and binding affinity. The Boc-protected amine allows for controlled deprotection and coupling in peptide-like synthesis, making it valuable in medicinal chemistry for building complex molecules with high enantiomeric purity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,220.00
inventory 1g
10-20 days ฿4,850.00
(S)-3-((tert-Butoxycarbonyl)amino)-3-(3-(trifluoromethyl)phenyl)propanoic acid
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Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and antidepressants. Its structure supports the development of selective serotonin reuptake inhibitors (SSRIs) due to the presence of the trifluoromethylphenyl group, which enhances metabolic stability and binding affinity. The Boc-protected amine allows for controlled deprotection and coupling in peptide-like synthesis, making it valuable in medicina

Used as a chiral intermediate in the synthesis of biologically active compounds, particularly in pharmaceuticals targeting central nervous system disorders and antidepressants. Its structure supports the development of selective serotonin reuptake inhibitors (SSRIs) due to the presence of the trifluoromethylphenyl group, which enhances metabolic stability and binding affinity. The Boc-protected amine allows for controlled deprotection and coupling in peptide-like synthesis, making it valuable in medicinal chemistry for building complex molecules with high enantiomeric purity.

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