2-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid

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Reagent Code: #62293
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CAS Number 658683-23-9

science Other reagents with same CAS 658683-23-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.31 g/mol
Formula C₁₄H₁₉NO₄
inventory_2 Storage & Handling
Storage 2-8°C, dry, sealed

description Product Description

This compound is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the preparation of various active pharmaceutical ingredients (APIs) and drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functional group, makes it valuable in peptide synthesis and other complex molecular constructions. The Boc group is often used to protect amines during multi-step reactions, ensuring selective transformations. Additionally, the benzoic acid moiety can be further modified to create diverse chemical entities, contributing to the development of novel therapeutic agents. Its application is especially prominent in the synthesis of compounds targeting specific biological pathways or receptors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿7,011.00
inventory 100mg
10-20 days ฿3,951.00

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2-(1-((tert-Butoxycarbonyl)amino)ethyl)benzoic acid
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This compound is primarily used as an intermediate in organic synthesis, particularly in the pharmaceutical industry. It plays a key role in the preparation of various active pharmaceutical ingredients (APIs) and drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid functional group, makes it valuable in peptide synthesis and other complex molecular constructions. The Boc group is often used to protect amines during multi-step reactions, ensuring selective transformations. Additionally, the benzoic acid moiety can be further modified to create diverse chemical entities, contributing to the development of novel therapeutic agents. Its application is especially prominent in the synthesis of compounds targeting specific biological pathways or receptors.
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