(S)-1-Benzyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate
95%
Reagent
Code: #104384
CAS Number
132245-78-4
blur_circular Chemical Specifications
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Molecular Information
Weight
351.39 g/mol
Formula
C₁₈H₂₅NO₆
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Registry Numbers
MDL Number
MFCD13184783
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Storage & Handling
Storage
room temperature
description Product Description
This compound is primarily utilized in the synthesis of peptides and other organic molecules, serving as a key intermediate in the production of complex pharmaceutical compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable in peptide chemistry, where selective protection and deprotection of functional groups are essential. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the benzyl ester moiety provides stability during synthetic processes and can be cleaved through hydrogenation when needed. This chemical is often employed in the development of biologically active molecules, including potential drug candidates, due to its ability to facilitate precise and efficient chemical transformations. Its application is particularly prominent in the field of medicinal chemistry, where it aids in the creation of novel therapeutic agents.
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(S)-1-Benzyl 5-methyl 2-((tert-butoxycarbonyl)amino)pentanedioate
This compound is primarily utilized in the synthesis of peptides and other organic molecules, serving as a key intermediate in the production of complex pharmaceutical compounds. Its structure, featuring a tert-butoxycarbonyl (Boc) protecting group, makes it particularly valuable in peptide chemistry, where selective protection and deprotection of functional groups are essential. The Boc group can be easily removed under mild acidic conditions, allowing for further functionalization of the molecule. Additionally, the benzyl ester moiety provides stability during synthetic processes and can be cleaved through hydrogenation when needed. This chemical is often employed in the development of biologically active molecules, including potential drug candidates, due to its ability to facilitate precise and efficient chemical transformations. Its application is particularly prominent in the field of medicinal chemistry, where it aids in the creation of novel therapeutic agents.
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