(S)-4-(1-Amino-2-hydroxyethyl)phenol hydrochloride

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Reagent Code: #113805
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CAS Number 763139-04-4

science Other reagents with same CAS 763139-04-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 189.64 g/mol
Formula C₂₀H₁₉N₃O₄
badge Registry Numbers
MDL Number MFCD18375671
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in the synthesis of chiral pharmaceutical intermediates, particularly in the development of beta-adrenergic receptor agonists. It serves as a key building block in the production of medications targeting respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Additionally, it is employed in research for designing enantiomerically pure compounds, contributing to the study of stereochemistry in drug development. Its application extends to organic synthesis where it aids in creating complex molecules with specific biological activities.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿11,952.00
inventory 100mg
10-20 days ฿5,976.00

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(S)-4-(1-Amino-2-hydroxyethyl)phenol hydrochloride
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This compound is primarily utilized in the synthesis of chiral pharmaceutical intermediates, particularly in the development of beta-adrenergic receptor agonists. It serves as a key building block in the production of medications targeting respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Additionally, it is employed in research for designing enantiomerically pure compounds, contributing to the study of stereochemistry in drug development. Its application extends to

This compound is primarily utilized in the synthesis of chiral pharmaceutical intermediates, particularly in the development of beta-adrenergic receptor agonists. It serves as a key building block in the production of medications targeting respiratory conditions such as asthma and chronic obstructive pulmonary disease (COPD). Additionally, it is employed in research for designing enantiomerically pure compounds, contributing to the study of stereochemistry in drug development. Its application extends to organic synthesis where it aids in creating complex molecules with specific biological activities.

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