155779-80-9

Basic information

• Product Name: (4S)-3-<(3S)-1-oxo-3-phenylbutyl>-4-(1-methylethyl)-2-oxazolidinone
• CAS NO: 155779-80-9
• Molecular Weight: 275.348
• Mol File: 155779-80-9.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (4S)-3-<(3S)-1-oxo-3-phenylbutyl>-4-(1-methylethyl)-2-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (4S)-3-<(3S)-1-oxo-3-phenylbutyl>-4-(1-methylethyl)-2-oxazolidinone(155779-80-9)
• EPA Substance Registry System: (4S)-3-<(3S)-1-oxo-3-phenylbutyl>-4-(1-methylethyl)-2-oxazolidinone(155779-80-9)

Safety Data

• Hazardous Substances Data: 155779-80-9(Hazardous Substances Data)

Upstream product

• 90719-29-2 (4S)-3-((E)-2-butenoyl)-4-(1-methylethyl)-2-oxazolidinone 
• 98-80-6 phenylboronic acid 
• 17016-83-0 (4S)-4-isopropyl-1,3-oxazolidin-2-one 
• 591-51-5 phenyllithium 
• 68679-84-5 (S)-3-phenyl butyric acid chloride 

Downstream Products

• 155896-57-4 (4S)-3-<(2S,3S)-1-oxo-2-<<(2-phenylethyl)thio>methyl>-3-phenylbutyl>-4-(1-methylethyl)-2-oxazolidinone 

Relevant articles and documents

Palladium-Catalyzed Diastereoselective Synthesis of 3-Arylbutanoic Acid Derivatives

The first palladium-catalyzed diastereoselective conjugate addition of arylboronic acids to chiral imides is reported. The catalytic system employing 4-tert-butyloxazolidin-2-one as the chiral auxiliary in a mixed solvent system of MeOH/H2O (1:3) under an air atmosphere provides the optically active 3-arylbutanoic acid derivatives in excellent yields with high diastereoselectivity.

New dual inhibitors of neutral endopeptidase and angiotensin-converting enzyme: Rational design, bioavailability, and pharmacological responses in experimental hypertension

In the treatment of cardiovascular diseases, it could be of therapeutic interest to associate the hypotensive effects resulting from the inhibition of angiotensin II formation, ensured by endothelial angiotensin-converting enzyme (ACE), with the diuretic