Methyl 2-(4-bromobenzyl)-3-((tert-butoxycarbonyl)amino)propanoate

≥95%

Reagent Code: #41684
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CAS Number 886366-46-7

science Other reagents with same CAS 886366-46-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 372.25 g/mol
Formula C₁₆H₂₂BrNO₄
badge Registry Numbers
MDL Number MFCD08061215
thermostat Physical Properties
Boiling Point 458.8±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Density 1.298g/cm3
Storage Room temperature, dry and sealed

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of peptide-based drugs, where the tert-butoxycarbonyl (Boc) group acts as a protective group for the amine functionality during synthesis. The presence of the bromobenzyl moiety allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Its application is significant in the design and synthesis of bioactive compounds, including potential therapeutic agents targeting specific biological pathways.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿11,637.00
100mg
10-20 days ฿5,814.00

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Methyl 2-(4-bromobenzyl)-3-((tert-butoxycarbonyl)amino)propanoate
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This compound is primarily utilized in organic synthesis as a key intermediate in the production of more complex molecules, particularly in pharmaceutical research. It serves as a building block for the development of peptide-based drugs, where the tert-butoxycarbonyl (Boc) group acts as a protective group for the amine functionality during synthesis. The presence of the bromobenzyl moiety allows for further functionalization through cross-coupling reactions, enabling the creation of diverse chemical structures. Its application is significant in the design and synthesis of bioactive compounds, including potential therapeutic agents targeting specific biological pathways.
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