(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid

≥95%

Reagent Code: #38097
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CAS Number 98628-27-4

science Other reagents with same CAS 98628-27-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.36 g/mol
Formula C₁₆H₂₃NO₄
badge Registry Numbers
MDL Number MFCD04117840
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid is primarily used in the field of peptide synthesis. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during the peptide chain assembly process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. The Boc protection can be selectively removed under acidic conditions, allowing for further elongation of the peptide chain without affecting other functional groups. Additionally, its phenylpentanoic acid moiety contributes to the structural diversity of synthesized peptides, making it useful in the development of bioactive peptides, peptidomimetics, and pharmaceutical agents. Its application extends to research in drug discovery, where it aids in the creation of compounds with potential therapeutic effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿5,760.00
inventory 100mg
10-20 days ฿2,880.00

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(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid
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(S)-2-((tert-Butoxycarbonyl)amino)-5-phenylpentanoic acid is primarily used in the field of peptide synthesis. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during the peptide chain assembly process. This compound is particularly valuable in solid-phase peptide synthesis (SPPS), enabling the stepwise construction of peptides with high precision. The Boc protection can be selectively removed under acidic conditions, allowing for further elongation of the peptide chain without affecting other functional groups. Additionally, its phenylpentanoic acid moiety contributes to the structural diversity of synthesized peptides, making it useful in the development of bioactive peptides, peptidomimetics, and pharmaceutical agents. Its application extends to research in drug discovery, where it aids in the creation of compounds with potential therapeutic effects.
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