(S)-5-(Allyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid

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Reagent Code: #38559
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CAS Number 132286-79-4

science Other reagents with same CAS 132286-79-4

blur_circular Chemical Specifications

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Weight 287.3089 g/mol
Formula C₁₃H₂₁NO₆
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MDL Number MFCD00273402
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description Product Description

Used primarily in the synthesis of peptides and complex organic molecules, this compound serves as a key intermediate in pharmaceutical research. Its structure, featuring both a Boc-protected amine and a carboxylic acid group, makes it valuable for constructing peptide chains with specific stereochemistry. The allyloxy group allows for further functionalization through reactions like deprotection or cross-coupling, enabling the creation of diverse bioactive compounds. It is particularly useful in developing drug candidates targeting enzymes or receptors, where precise molecular architecture is critical. Additionally, its application extends to material science, where it can be incorporated into polymers or coatings for specialized properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿747.00

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(S)-5-(Allyloxy)-2-((tert-butoxycarbonyl)amino)-5-oxopentanoic acid
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Used primarily in the synthesis of peptides and complex organic molecules, this compound serves as a key intermediate in pharmaceutical research. Its structure, featuring both a Boc-protected amine and a carboxylic acid group, makes it valuable for constructing peptide chains with specific stereochemistry. The allyloxy group allows for further functionalization through reactions like deprotection or cross-coupling, enabling the creation of diverse bioactive compounds. It is particularly useful in develop

Used primarily in the synthesis of peptides and complex organic molecules, this compound serves as a key intermediate in pharmaceutical research. Its structure, featuring both a Boc-protected amine and a carboxylic acid group, makes it valuable for constructing peptide chains with specific stereochemistry. The allyloxy group allows for further functionalization through reactions like deprotection or cross-coupling, enabling the creation of diverse bioactive compounds. It is particularly useful in developing drug candidates targeting enzymes or receptors, where precise molecular architecture is critical. Additionally, its application extends to material science, where it can be incorporated into polymers or coatings for specialized properties.

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