(S)-2-(4-(tert-Butyl)phenyl)-2-(methylamino)ethanol

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Reagent Code: #84862
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CAS Number 1213971-03-9

science Other reagents with same CAS 1213971-03-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.31 g/mol
Formula C₁₃H₂₁NO
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MDL Number MFCD09828096
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, inert gas

description Product Description

This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of certain beta-adrenergic receptor agonists, which are essential in treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral nature allows for the creation of enantiomerically pure drugs, enhancing efficacy and reducing side effects. Additionally, it finds application in organic synthesis for constructing complex molecular structures, particularly in asymmetric synthesis, where precise control over stereochemistry is crucial.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿25,340.00
inventory 100mg
10-20 days ฿16,890.00
inventory 1g
10-20 days ฿68,550.00

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(S)-2-(4-(tert-Butyl)phenyl)-2-(methylamino)ethanol
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This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of certain beta-adrenergic receptor agonists, which are essential in treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral nature allows for the creation of enantiomerically pure drugs, enhancing efficacy and reducing side effects. Additionally, it finds application in organic synthesi

This compound is primarily utilized in the synthesis of chiral molecules, particularly in the pharmaceutical industry. It serves as a key intermediate in the production of certain beta-adrenergic receptor agonists, which are essential in treating respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Its chiral nature allows for the creation of enantiomerically pure drugs, enhancing efficacy and reducing side effects. Additionally, it finds application in organic synthesis for constructing complex molecular structures, particularly in asymmetric synthesis, where precise control over stereochemistry is crucial.

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