(S)-3-((tert-Butoxycarbonyl)amino)-4-(naphthalen-1-yl)butanoic acid

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Reagent Code: #60703
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CAS Number 219297-09-3

science Other reagents with same CAS 219297-09-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 329.39 g/mol
Formula C₁₉H₂₃NO₄
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MDL Number MFCD01076282
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the development of biologically active compounds. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting specific enzymes or receptors. Its structure, featuring a naphthalene group, makes it valuable in creating molecules with enhanced binding affinity and selectivity. Additionally, it is utilized in research for designing inhibitors or modulators of protein-protein interactions, contributing to drug discovery efforts in areas such as cancer, inflammation, and infectious diseases. Its tert-butoxycarbonyl (Boc) protecting group allows for controlled deprotection during synthetic processes, ensuring precise construction of complex molecules.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,375.00

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(S)-3-((tert-Butoxycarbonyl)amino)-4-(naphthalen-1-yl)butanoic acid
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This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the development of biologically active compounds. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting specific enzymes or receptors. Its structure, featuring a naphthalene group, makes it valuable in creating molecules with enhanced binding affinity and selectivity. Additionally, it is utilized in research for designing inhibitors or modulators of protein-prote
This chemical is primarily used in the synthesis of peptides and peptidomimetics, particularly in the development of biologically active compounds. It serves as a key intermediate in the production of pharmaceutical agents, especially those targeting specific enzymes or receptors. Its structure, featuring a naphthalene group, makes it valuable in creating molecules with enhanced binding affinity and selectivity. Additionally, it is utilized in research for designing inhibitors or modulators of protein-protein interactions, contributing to drug discovery efforts in areas such as cancer, inflammation, and infectious diseases. Its tert-butoxycarbonyl (Boc) protecting group allows for controlled deprotection during synthetic processes, ensuring precise construction of complex molecules.
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