(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-fluoro-4-hydroxyphenyl)propanoic acid

95%

Reagent Code: #38102
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CAS Number 125218-32-8

science Other reagents with same CAS 125218-32-8

blur_circular Chemical Specifications

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Weight 299.2948 g/mol
Formula C₁₄H₁₈FNO₅
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description Product Description

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs. Its structure, featuring a Boc-protected amino group and a fluorinated aromatic ring, makes it valuable for creating molecules with specific biological activities. It is often employed in the production of enzyme inhibitors or receptor modulators, where the fluorine atom enhances binding affinity and metabolic stability. Additionally, the hydroxyl group on the phenyl ring allows for further functionalization, enabling the design of complex drug candidates. Its application is significant in medicinal chemistry for targeting diseases such as cancer, inflammation, or neurological disorders.

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inventory 100mg
10-20 days ฿7,533.00

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(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-fluoro-4-hydroxyphenyl)propanoic acid
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This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs. Its structure, featuring a Boc-protected amino group and a fluorinated aromatic ring, makes it valuable for creating molecules with specific biological activities. It is often employed in the production of enzyme inhibitors or receptor modulators, where the fluorine atom enhances binding affinity and metabolic stability. Additionally, the hydroxyl group on the phenyl r

This compound is primarily used in the synthesis of pharmaceutical intermediates, particularly in the development of peptide-based drugs. Its structure, featuring a Boc-protected amino group and a fluorinated aromatic ring, makes it valuable for creating molecules with specific biological activities. It is often employed in the production of enzyme inhibitors or receptor modulators, where the fluorine atom enhances binding affinity and metabolic stability. Additionally, the hydroxyl group on the phenyl ring allows for further functionalization, enabling the design of complex drug candidates. Its application is significant in medicinal chemistry for targeting diseases such as cancer, inflammation, or neurological disorders.

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