2-((tert-Butoxycarbonyl)amino)-3,3-diphenylpropanoic acid

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Reagent Code: #104449
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CAS Number 119363-63-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.40 g/mol
Formula C₂₀H₂₃NO₄
badge Registry Numbers
MDL Number MFCD00797562
thermostat Physical Properties
Melting Point 133 °C
Boiling Point 502.7±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.167±0.06 g/cm3(Predicted)
Storage Room temperature, sealed, dry

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in the development of peptides and pharmaceuticals. It serves as a key intermediate in the preparation of various biologically active molecules. The tert-butoxycarbonyl (Boc) group in the molecule acts as a protective group for amines, which is crucial during multi-step synthetic processes. This protection ensures that the amine functionality remains intact while other parts of the molecule undergo chemical reactions. Additionally, its diphenylpropanoic acid structure contributes to the stability and rigidity of the compounds being synthesized, making it valuable in the design of drugs that require specific structural configurations for activity. Its application is especially significant in the synthesis of compounds targeting neurological and inflammatory diseases, where precise molecular architecture is essential for efficacy.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days $83.35
inventory 250mg
10-20 days $177.81
inventory 1g
10-20 days $450.07
2-((tert-Butoxycarbonyl)amino)-3,3-diphenylpropanoic acid
This compound is primarily utilized in the field of organic synthesis, particularly in the development of peptides and pharmaceuticals. It serves as a key intermediate in the preparation of various biologically active molecules. The tert-butoxycarbonyl (Boc) group in the molecule acts as a protective group for amines, which is crucial during multi-step synthetic processes. This protection ensures that the amine functionality remains intact while other parts of the molecule undergo chemical reactions. Additionally, its diphenylpropanoic acid structure contributes to the stability and rigidity of the compounds being synthesized, making it valuable in the design of drugs that require specific structural configurations for activity. Its application is especially significant in the synthesis of compounds targeting neurological and inflammatory diseases, where precise molecular architecture is essential for efficacy.
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