(R)-3-(Boc-amino)-3-(3-methoxyphenyl)propionic acid

98%

Reagent Code: #52986
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CAS Number 500788-86-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
badge Registry Numbers
MDL Number MFCD03427937
thermostat Physical Properties
Melting Point 106-108 °C
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of chiral molecules. Its structure, featuring a Boc-protected amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs). It is often employed in peptide synthesis and the creation of complex organic molecules, where its chiral center ensures the desired stereochemistry in the final product. Additionally, it serves as a building block in the preparation of compounds targeting neurological and psychiatric disorders, leveraging its methoxyphenyl group for specific receptor interactions. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of new drug candidates with improved efficacy and selectivity.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿4,221.00
inventory 1g
10-20 days ฿8,307.00
(R)-3-(Boc-amino)-3-(3-methoxyphenyl)propionic acid
This compound is primarily used in the synthesis of pharmaceuticals, particularly in the development of chiral molecules. Its structure, featuring a Boc-protected amino group and a methoxyphenyl moiety, makes it a valuable intermediate in the production of active pharmaceutical ingredients (APIs). It is often employed in peptide synthesis and the creation of complex organic molecules, where its chiral center ensures the desired stereochemistry in the final product. Additionally, it serves as a building block in the preparation of compounds targeting neurological and psychiatric disorders, leveraging its methoxyphenyl group for specific receptor interactions. Its application extends to research and development in medicinal chemistry, where it aids in the exploration of new drug candidates with improved efficacy and selectivity.
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