3-((Tert-butoxycarbonyl)amino)-3-(4-ethylphenyl)propanoic acid

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Reagent Code: #242840
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CAS Number 284493-61-4

science Other reagents with same CAS 284493-61-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.36 g/mol
Formula C₁₆H₂₃NO₄
badge Registry Numbers
MDL Number MFCD02090703
thermostat Physical Properties
Boiling Point 451.4±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.120±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and peptide-based drugs. This compound features a tert-butoxycarbonyl (Boc) protecting group on the amino functionality, which enables selective modification and coupling reactions while preventing unwanted side reactions during synthesis. The Boc group can be easily removed under mild acidic conditions, making it highly suitable for constructing complex molecular structures in medicinal chemistry. Commonly employed in research for designing enzyme inhibitors or receptor modulators, and in the production of therapeutics for chronic diseases such as antivirals or diabetes treatments, due to its functional groups that facilitate molecular diversification.

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inventory 1g
10-20 days $1,812.67

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3-((Tert-butoxycarbonyl)amino)-3-(4-ethylphenyl)propanoic acid
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and peptide-based drugs. This compound features a tert-butoxycarbonyl (Boc) protecting group on the amino functionality, which enables selective modification and coupling reactions while preventing unwanted side reactions during synthesis. The Boc group can be easily removed under mild acidic conditions, making it highly suitable for constructing complex molecular structures in med

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules and peptide-based drugs. This compound features a tert-butoxycarbonyl (Boc) protecting group on the amino functionality, which enables selective modification and coupling reactions while preventing unwanted side reactions during synthesis. The Boc group can be easily removed under mild acidic conditions, making it highly suitable for constructing complex molecular structures in medicinal chemistry. Commonly employed in research for designing enzyme inhibitors or receptor modulators, and in the production of therapeutics for chronic diseases such as antivirals or diabetes treatments, due to its functional groups that facilitate molecular diversification.

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