3-Amino-3-(2-chlorophenyl)propanoic acid

98%

Reagent Code: #44884
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CAS Number 68208-20-8

science Other reagents with same CAS 68208-20-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.6300 g/mol
Formula C₉H₁₀ClNO₂
badge Registry Numbers
MDL Number MFCD01871299
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description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring both an amino group and a chlorophenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the production of compounds targeting central nervous system disorders, such as anticonvulsants or anxiolytics, due to its ability to interact with specific biological receptors. Additionally, it serves as a precursor in the synthesis of chiral molecules, where its stereochemistry is leveraged to create enantiomerically pure drugs. Its application extends to research settings, where it is used to study structure-activity relationships in drug design and optimization.

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Test Parameter Specification
Appearance White to Yellow solid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,260.00

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3-Amino-3-(2-chlorophenyl)propanoic acid
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This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring both an amino group and a chlorophenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the production of compounds targeting central nervous system disorders, such as anticonvulsants or anxiolytics, due to its ability to interact with specific biological r

This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs) for therapeutic drugs. Its structure, featuring both an amino group and a chlorophenyl moiety, makes it a valuable building block in medicinal chemistry. It is often employed in the production of compounds targeting central nervous system disorders, such as anticonvulsants or anxiolytics, due to its ability to interact with specific biological receptors. Additionally, it serves as a precursor in the synthesis of chiral molecules, where its stereochemistry is leveraged to create enantiomerically pure drugs. Its application extends to research settings, where it is used to study structure-activity relationships in drug design and optimization.

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