2-Amino-2-phenylpropanoic acid

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Reagent Code: #42562
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CAS Number 565-07-1

science Other reagents with same CAS 565-07-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 165.19 g/mol
Formula C₉H₁₁NO₂
badge Registry Numbers
MDL Number MFCD00195631
thermostat Physical Properties
Boiling Point 298.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, away from light, stored in an inert gas

description Product Description

2-Amino-2-phenylpropanoic acid is a synthetic amino acid analog primarily utilized as a key intermediate in pharmaceutical synthesis. It is employed in the development of various therapeutic agents, including enzyme inhibitors and peptide mimetics, due to its unique quaternary alpha-carbon structure. The compound's chirality makes it particularly useful for producing enantiomerically pure drugs. Additionally, it is applied in biochemical research to investigate molecular interactions, protein folding, and drug-receptor binding, advancing medicinal chemistry.

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Test Parameter Specification
Appearance White to off-white to yellow solid
Purity (%) 94.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,519.00
inventory 250mg
10-20 days ฿5,697.00
inventory 1g
10-20 days ฿14,472.00

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2-Amino-2-phenylpropanoic acid
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2-Amino-2-phenylpropanoic acid is a synthetic amino acid analog primarily utilized as a key intermediate in pharmaceutical synthesis. It is employed in the development of various therapeutic agents, including enzyme inhibitors and peptide mimetics, due to its unique quaternary alpha-carbon structure. The compound's chirality makes it particularly useful for producing enantiomerically pure drugs. Additionally, it is applied in biochemical research to investigate molecular interactions, protein folding, an

2-Amino-2-phenylpropanoic acid is a synthetic amino acid analog primarily utilized as a key intermediate in pharmaceutical synthesis. It is employed in the development of various therapeutic agents, including enzyme inhibitors and peptide mimetics, due to its unique quaternary alpha-carbon structure. The compound's chirality makes it particularly useful for producing enantiomerically pure drugs. Additionally, it is applied in biochemical research to investigate molecular interactions, protein folding, and drug-receptor binding, advancing medicinal chemistry.

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