(S)-2-((tert-Butoxycarbonyl)amino)-5-(dimethylamino)-5-oxopentanoic acid

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Reagent Code: #57136
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CAS Number 72449-42-4

science Other reagents with same CAS 72449-42-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 274.31 g/mol
Formula C₁₂H₂₂N₂O₅
badge Registry Numbers
MDL Number MFCD29920880
thermostat Physical Properties
Boiling Point 460.4±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.150±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides and proteins, particularly in research and pharmaceutical development. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino function, preventing unwanted reactions during the synthesis process. The dimethylamide group (from the 5-(dimethylamino)-5-oxo moiety) enhances solubility and can influence the reactivity of the compound. Its application is crucial in medicinal chemistry for designing peptide-based drugs, enzyme inhibitors, and other bioactive molecules. Additionally, it is utilized in the study of protein folding and structure-function relationships due to its ability to mimic natural amino acids while offering controlled reactivity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,572.00
inventory 250mg
10-20 days ฿7,623.00
inventory 1g
10-20 days ฿20,574.00

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(S)-2-((tert-Butoxycarbonyl)amino)-5-(dimethylamino)-5-oxopentanoic acid
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This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides and proteins, particularly in research and pharmaceutical development. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino function, preventing unwanted reactions during the synthesis process. The dimethylamide group (from the 5-(dimethylamino)-5-oxo moiety) enhances solubility and can influence the reactivity of the compound. Its

This compound is primarily used in peptide synthesis as a protected amino acid derivative. It serves as a building block for creating complex peptides and proteins, particularly in research and pharmaceutical development. The tert-butoxycarbonyl (Boc) group acts as a protective group for the amino function, preventing unwanted reactions during the synthesis process. The dimethylamide group (from the 5-(dimethylamino)-5-oxo moiety) enhances solubility and can influence the reactivity of the compound. Its application is crucial in medicinal chemistry for designing peptide-based drugs, enzyme inhibitors, and other bioactive molecules. Additionally, it is utilized in the study of protein folding and structure-function relationships due to its ability to mimic natural amino acids while offering controlled reactivity.

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