(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-chloro-3-fluorophenyl)propanoic acid

95%

Reagent Code: #38104
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CAS Number 1629658-28-1

science Other reagents with same CAS 1629658-28-1

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Weight 317.7405 g/mol
Formula C₁₄H₁₇ClFNO₄
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MDL Number MFCD30457720
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This chemical is primarily used in the field of pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. It serves as a key intermediate in the production of compounds that target specific biological pathways, such as enzyme inhibitors or receptor modulators. Its structure, featuring a Boc-protected amino group and a chloro-fluorophenyl moiety, makes it valuable for creating molecules with enhanced stability and binding affinity. Additionally, it is utilized in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Its applications also extend to the development of potential treatments for diseases involving protein-protein interactions or metabolic disorders.

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inventory 100mg
10-20 days ฿19,926.00

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(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-chloro-3-fluorophenyl)propanoic acid
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This chemical is primarily used in the field of pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. It serves as a key intermediate in the production of compounds that target specific biological pathways, such as enzyme inhibitors or receptor modulators. Its structure, featuring a Boc-protected amino group and a chloro-fluorophenyl moiety, makes it valuable for creating molecules with enhanced stability and binding affinity. Additionally, it is utilized in the stud
This chemical is primarily used in the field of pharmaceutical research and development, particularly in the synthesis of peptide-based drugs. It serves as a key intermediate in the production of compounds that target specific biological pathways, such as enzyme inhibitors or receptor modulators. Its structure, featuring a Boc-protected amino group and a chloro-fluorophenyl moiety, makes it valuable for creating molecules with enhanced stability and binding affinity. Additionally, it is utilized in the study of structure-activity relationships (SAR) to optimize drug efficacy and selectivity. Its applications also extend to the development of potential treatments for diseases involving protein-protein interactions or metabolic disorders.
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