ethyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate

≥98%(HPLC)

Reagent Code: #57760
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CAS Number 37178-37-3

science Other reagents with same CAS 37178-37-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.24 g/mol
Formula C₁₁H₁₅NO₄
badge Registry Numbers
MDL Number MFCD00871210
thermostat Physical Properties
Boiling Point 394.2 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.278 g/cm3
Storage 2-8°C

description Product Description

This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly those targeting neurological and cardiovascular conditions. Its structure, featuring both amino and dihydroxyphenyl groups, makes it a valuable intermediate in the production of dopamine-related drugs, which are essential for treating Parkinson's disease and other dopamine-deficiency disorders. Additionally, it serves as a precursor in the development of antioxidants and anti-inflammatory medications, leveraging its phenolic properties to combat oxidative stress and inflammation in various therapeutic contexts. Its ester functionality also allows for further chemical modifications, enhancing its versatility in drug design and development.

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Test Parameter Specification
APPEARANCE light yellow liquid
Purity (%) 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿21,024.00

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ethyl (2S)-2-amino-3-(3,4-dihydroxyphenyl)propanoate
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This compound is primarily utilized in the synthesis of pharmaceutical agents, particularly those targeting neurological and cardiovascular conditions. Its structure, featuring both amino and dihydroxyphenyl groups, makes it a valuable intermediate in the production of dopamine-related drugs, which are essential for treating Parkinson's disease and other dopamine-deficiency disorders. Additionally, it serves as a precursor in the development of antioxidants and anti-inflammatory medications, leveraging its phenolic properties to combat oxidative stress and inflammation in various therapeutic contexts. Its ester functionality also allows for further chemical modifications, enhancing its versatility in drug design and development.
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