(S)-Ethyl3-(3-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate

98%

Reagent Code: #237745
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CAS Number 1159502-91-6

science Other reagents with same CAS 1159502-91-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.25 g/mol
Formula C₁₆H₂₂BrNO₄
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules that require high enantiomeric purity. Its structure supports the construction of complex peptides and peptidomimetics, making it valuable in medicinal chemistry for drug discovery. The presence of a bromophenyl group allows for further functionalization via cross-coupling reactions, enabling the introduction of diverse substituents during synthetic campaigns. Commonly employed in research settings for optimizing lead compounds in central nervous system agents and enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,970.00
inventory 250mg
10-20 days ฿8,290.00
inventory 5g
10-20 days ฿49,740.00
inventory 10g
10-20 days ฿61,240.00
inventory 1g
10-20 days ฿16,580.00
(S)-Ethyl3-(3-bromophenyl)-2-((tert-butoxycarbonyl)amino)propanoate
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Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules that require high enantiomeric purity. Its structure supports the construction of complex peptides and peptidomimetics, making it valuable in medicinal chemistry for drug discovery. The presence of a bromophenyl group allows for further functionalization via cross-coupling reactions, enabling the introduction of diverse substituents during synthetic campaigns. Commonly employ

Used as a chiral intermediate in the synthesis of pharmaceutical compounds, particularly in the development of bioactive molecules that require high enantiomeric purity. Its structure supports the construction of complex peptides and peptidomimetics, making it valuable in medicinal chemistry for drug discovery. The presence of a bromophenyl group allows for further functionalization via cross-coupling reactions, enabling the introduction of diverse substituents during synthetic campaigns. Commonly employed in research settings for optimizing lead compounds in central nervous system agents and enzyme inhibitors.

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