5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)- - Names and Identifiers
Name | 5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)-
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Synonyms | 5-Oxazolidinepropanoic acid, 3-[(1,1-diMethylethoxy)carbonyl]-4-[(2S)-2-[[4-Methoxy-3-(3-Methoxyprop 5-Oxazolidinepropanoic acid, 3-[(1,1-diMethylethoxy)carbonyl]-4-[(2S)-2-[[4-Methoxy-3-(3-Methoxypropoxy)phenyl]Methyl]-3-Methylbutyl]-2,2-diMethyl-α-(1-Methylethyl)-, (αS,4S,5S)- 5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)-
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CAS | 172900-88-8
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5-Oxazolidinepropanoic acid, 3-[(1,1-dimethylethoxy)carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy)phenyl]methyl]-3-methylbutyl]-2,2-dimethyl-α-(1-methylethyl)-, (αS,4S,5S)- - Introduction
(Αs, 4S,5S)-3-[(tert-butoxy) carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy) phenyl] methyl]-3-methylbutyl]-2, 2-Dimethyl-alpha-isopropyl-5-oxazolidinpropionic acid is an organic compound.
Nature:
-chemical formula: C30H44N2O6
-Molecular weight: 524.68g/mol
-Appearance: Colorless or white solid
-Melting Point: about 111-113 ° C
-Stability: stable, not easy to decompose when encountering light and heat
Use:
(αs, 4S,5S)-3-[(tert-butoxy) carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy) phenyl] methyl]-3-methylbutyl]-2, 2-Dimethyl-alpha-isopropyl-5-oxazolidinpropionic acid is an active ingredient commonly used in the pharmaceutical field. It has antiviral and anti-inflammatory activities and can be used to treat viral infections and inflammation-related diseases.
Method:
(αs, 4S,5S)-3-[(tert-butoxy) carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy) phenyl] methyl]-3-methylbutyl]-2, the specific preparation of 2-dimethyl-alpha-isopropyl-5-oxazolidinpropionic acid may be difficult to describe because of the organic synthesis techniques and specific reaction conditions involved. However, commonly used synthetic methods typically involve a series of chemical reactions and steps, including oxidation reactions, glycosidation reactions, acylation reactions, etc.
Safety Information:
(αs, 4S,5S)-3-[(tert-butoxy) carbonyl]-4-[(2S)-2-[[4-methoxy-3-(3-methoxypropoxy) phenyl] methyl]-3-methylbutyl]-2, the safety information for 2-dimethyl-alpha-isopropyl-5-oxazolidinpropionic acid may vary depending on national and regional requirements. For any chemical, strictly follow the safety procedures and pay attention to the following:
-Avoid inhalation, skin contact and ingestion, and try to avoid contact with skin and eyes
-Wear appropriate personal protective equipment such as chemical goggles, gloves and lab coats for use
-Use in a well-ventilated area and avoid operating in a confined space
-Store in a cool, dry, well-ventilated place, away from fire and oxidizing agents
-In case of inadvertent exposure, immediately flush the affected area with clean water and seek medical help
Last Update:2024-04-10 22:29:15