(R)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenyl)propanoic acid

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Reagent Code: #230851
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CAS Number 478183-69-6

science Other reagents with same CAS 478183-69-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.3 g/mol
Formula C₁₄H₁₈N₂O₆
badge Registry Numbers
MDL Number MFCD01317701
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its ortho-nitrophenyl group facilitates spectroscopic monitoring during coupling reactions, while the Boc-protected amine allows for controlled deprotection and further functionalization in peptide-like sequences. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to its stereochemical purity and functional group compatibility.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿37,800.00
inventory 5g
10-20 days ฿133,200.00

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(R)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenyl)propanoic acid
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Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its ortho-nitrophenyl group facilitates spectroscopic monitoring during coupling reactions, while the Boc-protected amine allows for controlled deprotection and further functionalization in peptide-like sequences. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to its stereochemical purity and functional gro

Used as a chiral building block in the synthesis of pharmaceutical intermediates, particularly in the development of protease inhibitors and other bioactive molecules. Its ortho-nitrophenyl group facilitates spectroscopic monitoring during coupling reactions, while the Boc-protected amine allows for controlled deprotection and further functionalization in peptide-like sequences. Commonly employed in asymmetric synthesis and solid-phase peptide synthesis due to its stereochemical purity and functional group compatibility.

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