(R)-3-((tert-Butoxycarbonyl)amino)pentanoic acid

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Reagent Code: #104261
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CAS Number 183990-60-5

science Other reagents with same CAS 183990-60-5

blur_circular Chemical Specifications

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Weight 217.26 g/mol
Formula C₁₀H₁₉NO₄
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MDL Number MFCD08166685
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description Product Description

This compound is primarily used in the synthesis of peptides and pharmaceuticals, where it serves as a building block for creating complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in organic synthesis, particularly in peptide coupling reactions. The Boc group can be easily removed under mild acidic conditions, allowing for selective deprotection in multi-step synthetic processes. Additionally, its chiral nature enables the production of enantiomerically pure compounds, which is crucial in the development of drugs with specific biological activities. It is also employed in research settings for studying enzyme mechanisms and designing inhibitors.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿16,092.00
inventory 250mg
10-20 days ฿8,073.00

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(R)-3-((tert-Butoxycarbonyl)amino)pentanoic acid
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This compound is primarily used in the synthesis of peptides and pharmaceuticals, where it serves as a building block for creating complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in organic synthesis, particularly in peptide coupling reactions. The Boc group can be easily removed under mild acidic conditions, allowing for selective deprotection in multi-step synthetic processes. Additionally, its chiral nature enables the production of enantiome

This compound is primarily used in the synthesis of peptides and pharmaceuticals, where it serves as a building block for creating complex molecules. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it valuable in organic synthesis, particularly in peptide coupling reactions. The Boc group can be easily removed under mild acidic conditions, allowing for selective deprotection in multi-step synthetic processes. Additionally, its chiral nature enables the production of enantiomerically pure compounds, which is crucial in the development of drugs with specific biological activities. It is also employed in research settings for studying enzyme mechanisms and designing inhibitors.

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