(S)-2-Amino-2-(p-tolyl)ethanol

95%

Reagent Code: #38241
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CAS Number 327183-90-4

science Other reagents with same CAS 327183-90-4

blur_circular Chemical Specifications

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Weight 151.2100 g/mol
Formula C₉H₁₃NO
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MDL Number MFCD12758127
inventory_2 Storage & Handling
Storage room temperature

description Product Description

This compound is primarily utilized in the synthesis of chiral pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs, where its stereochemistry plays a critical role in efficacy. It serves as a key intermediate in the development of enantiomerically pure compounds, ensuring high specificity in drug action. Additionally, it is employed in organic synthesis for constructing complex molecules with high stereochemical control, making it valuable in medicinal chemistry and drug discovery. Its application extends to research settings for studying enzyme-substrate interactions and chiral catalysis.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,733.00

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(S)-2-Amino-2-(p-tolyl)ethanol
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This compound is primarily utilized in the synthesis of chiral pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs, where its stereochemistry plays a critical role in efficacy. It serves as a key intermediate in the development of enantiomerically pure compounds, ensuring high specificity in drug action. Additionally, it is employed in organic synthesis for constructing complex molecules with high stereochemical control, making it valuable in medicinal chemistry a

This compound is primarily utilized in the synthesis of chiral pharmaceuticals, particularly in the production of β-blockers and other cardiovascular drugs, where its stereochemistry plays a critical role in efficacy. It serves as a key intermediate in the development of enantiomerically pure compounds, ensuring high specificity in drug action. Additionally, it is employed in organic synthesis for constructing complex molecules with high stereochemical control, making it valuable in medicinal chemistry and drug discovery. Its application extends to research settings for studying enzyme-substrate interactions and chiral catalysis.

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