(R)-2-Amino-1-phenylethanol

98%

Reagent Code: #104226
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CAS Number 2549-14-6

science Other reagents with same CAS 2549-14-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 137.18 g/mol
Formula C₈H₁₁NO
badge Registry Numbers
MDL Number MFCD00239406
thermostat Physical Properties
Melting Point 59-65°C (Lit.)
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. It serves as a key intermediate in the preparation of optically active compounds, enhancing the efficacy and specificity of the final drug products. Additionally, it is employed in asymmetric synthesis to create enantiomerically pure substances, which are crucial in developing drugs with reduced side effects and improved therapeutic outcomes. Its role in organic synthesis also extends to the creation of fine chemicals and agrochemicals, where chirality plays a significant role in biological activity.

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Test Parameter Specification
Appearance White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms To Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,790.00
inventory 5g
10-20 days ฿10,800.00

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(R)-2-Amino-1-phenylethanol
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. It serves as a key intermediate in the preparation of optically active compounds, enhancing the efficacy and specificity of the final drug products. Additionally, it is employed in asymmetric synthesis to create enantiomerically pure substances, which are crucial in developing drugs with reduced side effects and improved therapeutic outcomes. Its role in org

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the production of beta-blockers and other cardiovascular drugs. It serves as a key intermediate in the preparation of optically active compounds, enhancing the efficacy and specificity of the final drug products. Additionally, it is employed in asymmetric synthesis to create enantiomerically pure substances, which are crucial in developing drugs with reduced side effects and improved therapeutic outcomes. Its role in organic synthesis also extends to the creation of fine chemicals and agrochemicals, where chirality plays a significant role in biological activity.

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