(S)-Boc-γ,γ-diphenyl-β-Homoala-OH

≥98%(HPLC)

Reagent Code: #104645
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CAS Number 190190-50-2

science Other reagents with same CAS 190190-50-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 355.43 g/mol
Formula C₂₁H₂₅NO₄
badge Registry Numbers
MDL Number MFCD02094564
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group provides stability during peptide bond formation, preventing unwanted side reactions. It is particularly valuable in the preparation of complex peptide structures, enabling the incorporation of diphenylalanine-like motifs. This compound is also employed in medicinal chemistry for designing drug candidates, especially those targeting protein-protein interactions, due to its unique structural features. Additionally, it finds application in the development of chiral catalysts and ligands for asymmetric synthesis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿15,282.00
inventory 500mg
10-20 days ฿52,182.00
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(S)-Boc-γ,γ-diphenyl-β-Homoala-OH
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This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group provides stability during peptide bond formation, preventing unwanted side reactions. It is particularly valuable in the preparation of complex peptide structures, enabling the incorporation of diphenylalanine-like motifs. This compound is also employed in medicinal chemistry for designing drug candidates, especially those targeting pr

This chemical is primarily used in the synthesis of peptides and peptidomimetics, where it serves as a protected amino acid derivative. The Boc (tert-butoxycarbonyl) group provides stability during peptide bond formation, preventing unwanted side reactions. It is particularly valuable in the preparation of complex peptide structures, enabling the incorporation of diphenylalanine-like motifs. This compound is also employed in medicinal chemistry for designing drug candidates, especially those targeting protein-protein interactions, due to its unique structural features. Additionally, it finds application in the development of chiral catalysts and ligands for asymmetric synthesis.

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