(S)-Methyl 2-amino-3-(naphthalen-1-yl)propanoate hydrochloride

95%

Reagent Code: #87178
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CAS Number 63024-25-9

science Other reagents with same CAS 63024-25-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.74 g/mol
Formula C₁₄H₁₆ClNO₂
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MDL Number MFCD24434978
inventory_2 Storage & Handling
Storage room temperature, inert gas storage

description Product Description

This compound is primarily utilized in the pharmaceutical and research sectors. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular systems. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in peptide synthesis, where its naphthalene moiety can enhance binding affinity and stability in drug candidates. Researchers also use it to study receptor-ligand interactions, aiding in the design of novel therapeutic agents. Its hydrochloride form improves solubility, making it suitable for experimental and formulation purposes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,887.00
inventory 250mg
10-20 days ฿7,326.00
inventory 1g
10-20 days ฿18,270.00

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(S)-Methyl 2-amino-3-(naphthalen-1-yl)propanoate hydrochloride
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This compound is primarily utilized in the pharmaceutical and research sectors. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular systems. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in peptide synthesis, where its naphthalene moiety can enhance binding affinity and stability in drug
This compound is primarily utilized in the pharmaceutical and research sectors. It serves as a key intermediate in the synthesis of various biologically active molecules, particularly those targeting neurological and cardiovascular systems. Its chiral structure makes it valuable in the development of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in peptide synthesis, where its naphthalene moiety can enhance binding affinity and stability in drug candidates. Researchers also use it to study receptor-ligand interactions, aiding in the design of novel therapeutic agents. Its hydrochloride form improves solubility, making it suitable for experimental and formulation purposes.
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