3-(4-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate

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Reagent Code: #150999
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CAS Number 132067-41-5

science Other reagents with same CAS 132067-41-5

blur_circular Chemical Specifications

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Weight 358.23 g/mol
Formula C₁₅H₂₀BrNO₄
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MDL Number MFCD22418965
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide mimetic design, making it valuable in medicinal chemistry for creating enzyme inhibitors. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step organic syntheses. Commonly employed in research settings for constructing complex molecules requiring chiral alpha-amino acid derivatives with aromatic side chains.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,810.00
inventory 250mg
10-20 days ฿4,710.00
inventory 1g
10-20 days ฿9,510.00
inventory 5g
10-20 days ฿34,630.00

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3-(4-Bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide mimetic design, making it valuable in medicinal chemistry for creating enzyme inhibitors. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step organic syntheses. Commonly employed in research settings for constructing complex molecules requiring chiral alpha-amino acid der

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other bioactive molecules. Its structure supports peptide mimetic design, making it valuable in medicinal chemistry for creating enzyme inhibitors. The Boc-protected amine allows for selective deprotection and further functionalization in multi-step organic syntheses. Commonly employed in research settings for constructing complex molecules requiring chiral alpha-amino acid derivatives with aromatic side chains.

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