113806-28-3

Basic information

• Product Name: (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone
• Synonyms: (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone;(2R-trans)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone
• CAS NO: 113806-28-3
• Molecular Formula: C₁₇H₁₅NO₃
• Molecular Weight: 281.31
• Product Categories: Aromatics Compounds;Aromatics;Chiral Reagents;Heterocycles
• Mol File: 113806-28-3.mol

Chemical Properties

• Appearance: /
• Solubility: Dichloromethane, Ethyl Acetate, Methanol
• CAS DataBase Reference: (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone(CAS DataBase Reference)
• NIST Chemistry Reference: (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone(113806-28-3)
• EPA Substance Registry System: (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone(113806-28-3)

Safety Data

• Hazardous Substances Data: 113806-28-3(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Industry:
(2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone is used as a central nervous system agent for its potential therapeutic effects on neurological disorders and conditions. Its unique structure and chirality may contribute to its interaction with specific biological targets, offering a new avenue for drug development and treatment.
Used in Chemical Research:
As a chiral compound, (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone can be employed in the field of chemical research for the development of enantioselective synthesis methods and the study of stereochemistry in organic reactions. Its distinct stereochemistry and functional groups make it a valuable subject for exploring new synthetic pathways and understanding the role of chirality in chemical processes.
Used in Material Science:
The white solid nature of (2R,4S)-3-Benzoyl-4-methyl-2-phenyl-5-oxazolidinone may also find applications in material science, particularly in the development of new materials with specific properties. Its unique structure could be utilized in the creation of novel polymers, coatings, or other materials with tailored characteristics for various industrial applications.

Upstream product

• 100-52-7 benzaldehyde 
• 98-88-4 benzoyl chloride 
• 56-41-7 L-alanin 

Downstream Products

• 65-85-0 benzoic acid 
• 100-52-7 benzaldehyde 
• 189452-40-2 (1S,2S)-2-((2R,4S)-3-Benzoyl-4-methyl-5-oxo-2-phenyl-oxazolidin-4-yl)-cyclopropanecarboxylic acid methyl ester 
• 189452-43-5 (1R,2R)-2-((2R,4S)-3-Benzoyl-4-methyl-5-oxo-2-phenyl-oxazolidin-4-yl)-cyclopropanecarboxylic acid methyl ester 
• 189452-34-4 [2-((2R,4S)-3-Benzoyl-4-methyl-5-oxo-2-phenyl-oxazolidin-4-yl)-ethyl]-phosphonic acid diethyl ester 
• 189452-31-1 (2R,4S)-3-Benzoyl-4-(2-iodo-ethyl)-4-methyl-2-phenyl-oxazolidin-5-one 
• 216491-37-1 (2R,4S)-3-Benzoyl-4-(3-benzyloxy-benzyl)-4-methyl-2-phenyl-oxazolidin-5-one 
• 190393-72-7 (2S,4S)-3-benzoyl-4-methyl-4-(phthalimidomethyl)-2-phenyl-1,3-oxazolidin-5-one 
• 189452-25-3 (2R,4S)-3-benzoyl-4-bromoethyl-4-methyl-2-phenyl-1,3-oxazolidin-5-one 
• 189452-37-7 (E)-3-((2R,4S)-3-Benzoyl-4-methyl-5-oxo-2-phenyl-oxazolidin-4-yl)-acrylic acid methyl ester 
• 118995-18-9 (2R,4S)-3-Benzoyl-4-ethyl-4-methyl-2-phenyl-oxazolidin-5-one 

Relevant articles and documents

Synthesis of optically active imidazolines, azapenams, dioxocyclams, and bis-dioxocyclams

Optically active 4-methyl-4-carbomethoxy-Δ2-imidazoline was efficiently synthesized on a multigram scale. Photolysis with (methoxymethylcarbene)chromium complex produced the optically active azapenam in good yield and with high stereoselectivity. Acid-catalyzed dimerization followed by reduction produced the corresponding optically active dioxocyclam in good yield. Using a bis-carbene complex, an optically active bis-dioxocyclam was produced in excellent yield.