(R)-3-((tert-Butoxycarbonyl)amino)-3-(3-cyanophenyl)propanoic acid

97%

Reagent Code: #229479
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CAS Number 501015-21-0

science Other reagents with same CAS 501015-21-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 290.31 g/mol
Formula C₁₅H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD03427967
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptide-like chains with specific stereochemistry, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Commonly employed in solid-phase and solution-phase peptide synthesis where the Boc-protected amine allows for controlled deprotection and coupling steps. The nitrile group can be further modified to introduce heterocycles or other functional groups, expanding its utility in drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,530.00
inventory 250mg
10-20 days ฿5,980.00
inventory 1g
10-20 days ฿16,130.00
(R)-3-((tert-Butoxycarbonyl)amino)-3-(3-cyanophenyl)propanoic acid
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptide-like chains with specific stereochemistry, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Commonly employed in solid-phase and solution-phase peptide synthesis where the Boc-protected amine allows for controlled deprotection and coupling steps. The

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its structure supports the formation of peptide-like chains with specific stereochemistry, making it valuable in medicinal chemistry for optimizing drug potency and selectivity. Commonly employed in solid-phase and solution-phase peptide synthesis where the Boc-protected amine allows for controlled deprotection and coupling steps. The nitrile group can be further modified to introduce heterocycles or other functional groups, expanding its utility in drug discovery.

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