2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoic acid

95%

Reagent Code: #104455
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CAS Number 169870-82-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 231.29 g/mol
Formula C₁₁H₂₁NO₄
badge Registry Numbers
MDL Number MFCD00057782
thermostat Physical Properties
Boiling Point 350.0±25.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.063±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of peptides and pharmaceuticals. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during complex chemical reactions. This protection is crucial in multi-step synthesis processes, allowing for selective reactions without unwanted side interactions. Additionally, it is employed in the development of biologically active compounds, including drug candidates, due to its structural stability and compatibility with various reaction conditions. Its role in peptide synthesis makes it valuable in research and industrial applications aimed at creating therapeutic agents and studying protein structures.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿24,732.00
inventory 1g
10-20 days ฿12,600.00
inventory 250mg
10-20 days ฿6,300.00
2-((tert-butoxycarbonyl)amino)-3,3-dimethylbutanoic acid
This chemical is primarily used as an intermediate in organic synthesis, particularly in the production of peptides and pharmaceuticals. It serves as a protected amino acid derivative, where the tert-butoxycarbonyl (Boc) group safeguards the amino functionality during complex chemical reactions. This protection is crucial in multi-step synthesis processes, allowing for selective reactions without unwanted side interactions. Additionally, it is employed in the development of biologically active compounds, including drug candidates, due to its structural stability and compatibility with various reaction conditions. Its role in peptide synthesis makes it valuable in research and industrial applications aimed at creating therapeutic agents and studying protein structures.
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