(S)-2-Acetamido-3-(naphthalen-2-yl)propanoic acid

95%

Reagent Code: #57150
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CAS Number 37439-99-9

science Other reagents with same CAS 37439-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.28 g/mol
Formula C₁₅H₁₅NO₃
badge Registry Numbers
MDL Number MFCD03094597
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders and inflammatory conditions. Its structural features make it suitable for incorporation into peptide-based drugs, enhancing their binding affinity and specificity to target receptors. Additionally, it is explored in research for its potential role in inhibiting specific enzymes or proteins involved in disease pathways, contributing to the development of novel therapeutic strategies. Its application is also seen in the study of chiral molecules, where it aids in understanding stereochemistry and its impact on biological activity.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,285.00
inventory 1g
10-20 days ฿1,071.00
inventory 25g
10-20 days ฿12,483.00

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(S)-2-Acetamido-3-(naphthalen-2-yl)propanoic acid
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This compound is primarily utilized in the field of medicinal chemistry and drug development. It serves as a key intermediate in the synthesis of various pharmaceutical agents, particularly those targeting neurological disorders and inflammatory conditions. Its structural features make it suitable for incorporation into peptide-based drugs, enhancing their binding affinity and specificity to target receptors. Additionally, it is explored in research for its potential role in inhibiting specific enzymes or proteins involved in disease pathways, contributing to the development of novel therapeutic strategies. Its application is also seen in the study of chiral molecules, where it aids in understanding stereochemistry and its impact on biological activity.
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