(S)-Methyl 3-((tert-butoxycarbonyl)amino)-3-methyl-2-(((S)-1-phenylethyl)amino)butanoate

≥95%

Reagent Code: #38379
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CAS Number 1093192-06-3

science Other reagents with same CAS 1093192-06-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.45 g/mol
Formula C₁₉H₃₀N₂O₄
badge Registry Numbers
MDL Number MFCD27992079
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in an inert gas

description Product Description

This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral drugs, where its stereochemical properties are crucial for achieving the desired biological activity. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during multi-step syntheses, while the chiral centers allow for the creation of enantiomerically pure compounds. It is often employed in peptide chemistry and the development of enzyme inhibitors, leveraging its structural features to enhance drug efficacy and specificity. Additionally, it finds application in research focused on asymmetric synthesis, aiding in the study of stereoselective reactions and the development of novel therapeutic agents.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿12,501.00
inventory 250mg
10-20 days ฿4,167.00
inventory 100mg
10-20 days ฿2,493.00

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(S)-Methyl 3-((tert-butoxycarbonyl)amino)-3-methyl-2-(((S)-1-phenylethyl)amino)butanoate
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This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral drugs, where its stereochemical properties are crucial for achieving the desired biological activity. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during multi-step syntheses, while the chiral centers allow for the creation of enantiomerically pure compounds. It is often employed in peptide che

This compound is primarily used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of chiral drugs, where its stereochemical properties are crucial for achieving the desired biological activity. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactions during multi-step syntheses, while the chiral centers allow for the creation of enantiomerically pure compounds. It is often employed in peptide chemistry and the development of enzyme inhibitors, leveraging its structural features to enhance drug efficacy and specificity. Additionally, it finds application in research focused on asymmetric synthesis, aiding in the study of stereoselective reactions and the development of novel therapeutic agents.

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