(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid

98%

Reagent Code: #104367
label
Alias Boc-4-tert-butyl-Phe-OH
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CAS Number 143415-62-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 321.41 g/mol
Formula C₁₈H₂₇NO₄
badge Registry Numbers
MDL Number MFCD02094432
thermostat Physical Properties
Boiling Point 461.413°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of peptide-based compounds, particularly in the development of drugs targeting specific biological pathways. Its structure, featuring a tert-butyl group and a Boc-protected amino acid, makes it valuable for creating complex molecules with enhanced stability and bioavailability. Researchers often utilize it in the synthesis of protease inhibitors, receptor antagonists, and other therapeutic agents. Additionally, it is employed in the study of enzyme mechanisms and protein interactions due to its ability to mimic natural amino acids while providing steric and electronic modifications.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days €55.99
inventory 1g
10-20 days €112.46
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-(tert-butyl)phenyl)propanoic acid
This chemical is primarily used in the field of organic synthesis and pharmaceutical research. It serves as a key intermediate in the preparation of peptide-based compounds, particularly in the development of drugs targeting specific biological pathways. Its structure, featuring a tert-butyl group and a Boc-protected amino acid, makes it valuable for creating complex molecules with enhanced stability and bioavailability. Researchers often utilize it in the synthesis of protease inhibitors, receptor antagonists, and other therapeutic agents. Additionally, it is employed in the study of enzyme mechanisms and protein interactions due to its ability to mimic natural amino acids while providing steric and electronic modifications.
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