3-(2-Amino-2-carboxyethyl)benzoic acid hydrochloride

98%

Reagent Code: #44242
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CAS Number 80852-34-2

science Other reagents with same CAS 80852-34-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.6596 g/mol
Formula C₁₀H₁₂ClNO₄
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of peptides and other bioactive molecules. Its structure, featuring both amino and carboxylic acid functional groups, makes it a valuable building block for creating complex organic compounds. It is often employed in the preparation of drug intermediates, where its properties facilitate the formation of stable amide bonds. Additionally, it can be utilized in studies focused on enzyme inhibition or receptor binding due to its ability to mimic natural amino acids. Its hydrochloride form enhances solubility, making it suitable for use in aqueous-based reactions and biological assays.

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inventory 100mg
10-20 days ฿17,559.00

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3-(2-Amino-2-carboxyethyl)benzoic acid hydrochloride
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This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of peptides and other bioactive molecules. Its structure, featuring both amino and carboxylic acid functional groups, makes it a valuable building block for creating complex organic compounds. It is often employed in the preparation of drug intermediates, where its properties facilitate the formation of stable amide bonds. Additionally, it can be utilized in studies focused on enzyme inhibition or re

This compound is primarily used in pharmaceutical research and development, particularly in the synthesis of peptides and other bioactive molecules. Its structure, featuring both amino and carboxylic acid functional groups, makes it a valuable building block for creating complex organic compounds. It is often employed in the preparation of drug intermediates, where its properties facilitate the formation of stable amide bonds. Additionally, it can be utilized in studies focused on enzyme inhibition or receptor binding due to its ability to mimic natural amino acids. Its hydrochloride form enhances solubility, making it suitable for use in aqueous-based reactions and biological assays.

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