(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenyl)propanoic acid

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Reagent Code: #38087
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CAS Number 185146-84-3

science Other reagents with same CAS 185146-84-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.30 g/mol
Formula C₁₄H₁₈N₂O₆
badge Registry Numbers
MDL Number MFCD01317708
thermostat Physical Properties
Boiling Point 488°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed

description Product Description

This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amino group, ensuring selectivity during chemical reactions. Its nitrophenyl component can be involved in further functionalization or as a precursor for more complex molecules. It is often employed in organic and medicinal chemistry research for developing drug candidates, particularly in the creation of enzyme inhibitors or receptor-targeting agents. The compound’s structure allows for controlled deprotection and modification, making it valuable in multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 10g
10-20 days ฿32,886.00
inventory 5g
10-20 days ฿17,154.00
inventory 1g
10-20 days ฿3,429.00
inventory 250mg
10-20 days ฿1,368.00

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(S)-2-((tert-Butoxycarbonyl)amino)-3-(2-nitrophenyl)propanoic acid
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This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amino group, ensuring selectivity during chemical reactions. Its nitrophenyl component can be involved in further functionalization or as a precursor for more complex molecules. It is often employed in organic and medicinal chemistry research for developing drug candidates, particularly in the creat
This compound is primarily utilized in the synthesis of peptides and pharmaceuticals, where it serves as a protected amino acid derivative. The tert-butoxycarbonyl (Boc) group acts as a protective moiety for the amino group, ensuring selectivity during chemical reactions. Its nitrophenyl component can be involved in further functionalization or as a precursor for more complex molecules. It is often employed in organic and medicinal chemistry research for developing drug candidates, particularly in the creation of enzyme inhibitors or receptor-targeting agents. The compound’s structure allows for controlled deprotection and modification, making it valuable in multi-step synthetic processes.
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