(S)-3-Amino-3-(3-nitrophenyl)propanoic acid

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Reagent Code: #38437
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CAS Number 734529-57-8

science Other reagents with same CAS 734529-57-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 210.19 g/mol
Formula C₉H₁₀N₂O₄
badge Registry Numbers
MDL Number MFCD04113693
thermostat Physical Properties
Boiling Point 384.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

(S)-3-Amino-3-(3-nitrophenyl)propanoic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring both an amino group and a nitro-substituted phenyl ring, makes it a valuable building block for designing molecules with potential therapeutic effects. Researchers often employ it in the development of enzyme inhibitors, receptor modulators, and other drug candidates. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug design, enhancing the efficacy and selectivity of potential medications.

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Test Parameter Specification
Appearance Off-White Powder
Purity (%) 96.5-100%
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,034.00
inventory 10g
10-20 days ฿33,318.00
inventory 1g
10-20 days ฿5,112.00
inventory 5g
10-20 days ฿16,713.00

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(S)-3-Amino-3-(3-nitrophenyl)propanoic acid
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(S)-3-Amino-3-(3-nitrophenyl)propanoic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. It serves as a key intermediate in the synthesis of various biologically active compounds, particularly those targeting neurological and cardiovascular disorders. Its structure, featuring both an amino group and a nitro-substituted phenyl ring, makes it a valuable building block for designing molecules with potential therapeutic effects. Researchers often employ it in the development of enzyme inhibitors, receptor modulators, and other drug candidates. Additionally, its chiral nature allows for the exploration of stereospecific interactions in drug design, enhancing the efficacy and selectivity of potential medications.
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