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

95%

Reagent Code: #55931
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CAS Number 188256-28-2

science Other reagents with same CAS 188256-28-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 265.7353 g/mol
Formula C₁₄H₁₆ClNO₂
badge Registry Numbers
MDL Number MFCD24434602
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development. 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 production of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in the study of receptor-ligand interactions, aiding in the design of novel therapeutic agents. The compound’s naphthalene moiety contributes to its potential use in fluorescent labeling and imaging applications, particularly in cellular and molecular biology studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,653.00

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(R)-Methyl 2-amino-3-(naphthalen-1-yl)propanoate hydrochloride
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This compound is primarily utilized in the field of pharmaceutical research and development. 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 production of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in the study of receptor-ligand interactions, aiding in the design of novel therapeuti

This compound is primarily utilized in the field of pharmaceutical research and development. 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 production of enantiomerically pure drugs, ensuring higher efficacy and reduced side effects. Additionally, it is employed in the study of receptor-ligand interactions, aiding in the design of novel therapeutic agents. The compound’s naphthalene moiety contributes to its potential use in fluorescent labeling and imaging applications, particularly in cellular and molecular biology studies.

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