(S)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate

≥95%

Reagent Code: #38282
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CAS Number 1093192-07-4

science Other reagents with same CAS 1093192-07-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.30 g/mol
Formula C₁₁H₂₂N₂O₄
badge Registry Numbers
MDL Number MFCD16293742
inventory_2 Storage & Handling
Storage -20°C, protected from light and stored in an inert gas

description Product Description

This compound is primarily used in the synthesis of peptides and peptidomimetics, serving as a protected amino acid derivative. It is particularly valuable in organic and medicinal chemistry for constructing complex molecules, as the tert-butoxycarbonyl (Boc) group protects the amino functionality during reactions, preventing unwanted side reactions. It is often employed in the development of pharmaceuticals, especially in the production of drugs targeting specific biological pathways. Additionally, its chiral nature makes it useful in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. This chemical is also utilized in research for studying enzyme mechanisms and designing enzyme inhibitors.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,911.00
inventory 1g
10-20 days ฿34,614.00
inventory 250mg
10-20 days ฿13,851.00

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(S)-Methyl 2-amino-3-((tert-butoxycarbonyl)amino)-3-methylbutanoate
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This compound is primarily used in the synthesis of peptides and peptidomimetics, serving as a protected amino acid derivative. It is particularly valuable in organic and medicinal chemistry for constructing complex molecules, as the tert-butoxycarbonyl (Boc) group protects the amino functionality during reactions, preventing unwanted side reactions. It is often employed in the development of pharmaceuticals, especially in the production of drugs targeting specific biological pathways. Additionally, its chiral nature makes it useful in asymmetric synthesis, enabling the creation of enantiomerically pure compounds. This chemical is also utilized in research for studying enzyme mechanisms and designing enzyme inhibitors.
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