(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)propanoic acid

95%

Reagent Code: #235872
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CAS Number 479064-90-9

science Other reagents with same CAS 479064-90-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 299.75 g/mol
Formula C₁₄H₁₈ClNO₄
badge Registry Numbers
MDL Number MFCD03427922
thermostat Physical Properties
Melting Point 135 - 137 ℃
Boiling Point 453.9 ℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.243 g/cm3
Storage Room temperature

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 stereochemistry allows for selective interactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in peptide mimetics and medicinal chemistry research to build complex molecules with high specificity. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, facilitating its incorporation into larger molecular frameworks.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,630.00
inventory 250mg
10-20 days ฿5,270.00
inventory 1g
10-20 days ฿12,710.00
inventory 5g
10-20 days ฿36,470.00
inventory 10g
10-20 days ฿47,090.00
(S)-3-((tert-Butoxycarbonyl)amino)-3-(4-chlorophenyl)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 stereochemistry allows for selective interactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in peptide mimetics and medicinal chemistry research to build complex molecules with high specificity. The Boc-protected amine and carboxylic acid functionalities enable stepwise c

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its stereochemistry allows for selective interactions in asymmetric synthesis, making it valuable in creating enantiomerically pure drugs. Commonly employed in peptide mimetics and medicinal chemistry research to build complex molecules with high specificity. The Boc-protected amine and carboxylic acid functionalities enable stepwise coupling reactions, facilitating its incorporation into larger molecular frameworks.

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