4-[(tert-butoxycarbonyl)amino]-2-hydroxybenzoic acid

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Reagent Code: #46729
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CAS Number 184033-42-9

science Other reagents with same CAS 184033-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.25 g/mol
Formula C₁₂H₁₅NO₅
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the development of drugs, especially those targeting inflammation, pain, and other therapeutic areas. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during multi-step synthetic processes, ensuring selective reactions. Additionally, its hydroxyl and carboxylic acid functional groups make it versatile for further derivatization, enabling the creation of complex molecules with specific biological activities. Its application is also seen in peptide synthesis, where it aids in the controlled assembly of amino acids.

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inventory 1g
10-20 days ฿38,808.00

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4-[(tert-butoxycarbonyl)amino]-2-hydroxybenzoic acid
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This chemical is primarily utilized in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the development of drugs, especially those targeting inflammation, pain, and other therapeutic areas. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during multi-step synthetic processes, ensuring selective reactions. Additionally, its hydroxyl and carboxylic acid functional grou

This chemical is primarily utilized in organic synthesis, particularly in the preparation of pharmaceuticals and bioactive compounds. It serves as a key intermediate in the development of drugs, especially those targeting inflammation, pain, and other therapeutic areas. The tert-butoxycarbonyl (Boc) protecting group in the molecule is crucial for safeguarding the amino group during multi-step synthetic processes, ensuring selective reactions. Additionally, its hydroxyl and carboxylic acid functional groups make it versatile for further derivatization, enabling the creation of complex molecules with specific biological activities. Its application is also seen in peptide synthesis, where it aids in the controlled assembly of amino acids.

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