221293-02-3

Basic information

• Product Name: (R)-4-benzyl-3-((R)-4-methylhexanoyl)oxazolidin-2-one
• Synonyms: (R)-4-benzyl-3-((R)-4-methylhexanoyl)oxazolidin-2-one
• CAS NO: 221293-02-3
• Molecular Weight: 289.375
• Mol File: 221293-02-3.mol

Chemical Properties

• CAS DataBase Reference: (R)-4-benzyl-3-((R)-4-methylhexanoyl)oxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (R)-4-benzyl-3-((R)-4-methylhexanoyl)oxazolidin-2-one(221293-02-3)
• EPA Substance Registry System: (R)-4-benzyl-3-((R)-4-methylhexanoyl)oxazolidin-2-one(221293-02-3)

Safety Data

• Hazardous Substances Data: 221293-02-3(Hazardous Substances Data)

Upstream product

• 70432-01-8 (R)-4-methyl-hexanoyl chloride 
• 372504-89-7 (R)-4-benzyl-2-oxazolidinone lithium salt 
• 40217-17-2 (R)-4-(phenylmethyl)-2-oxazolidinone 
• 7540-51-4 (S)-3,7-dimethyl-6-octen-1-ol 
• 313653-16-6 methanesulfonic Acid (S)-3,7-dimethyl-oct-6-enyl Ester 
• 53353-03-0 (R)-(-)-2,6-dimethyl-2-octene 
• 52745-93-4 (4R)-4-methylhexanoic acid 

Downstream Products

• 446262-64-2 (4R)-4-benzyl-3-[(2S,4R)-2,4-dimethylhexanoyl]-1,3-oxazolidin-2-one 
• 221293-18-1 2-((1R,3R)-1-tert-Butoxycarbonylamino-3-methyl-pentyl)-5-(1H-indol-3-yl)-oxazole-4-carboxylic acid benzyl ester 
• 221293-19-2 2-((1R,3R)-1-Amino-3-methyl-pentyl)-5-(1H-indol-3-yl)-oxazole-4-carboxylic acid benzyl ester 
• 221293-03-4 (R)-3-((2R,4R)-2-Azido-4-methyl-hexanoyl)-4-benzyl-oxazolidin-2-one 

Relevant articles and documents

Synthesis of the Entomopathogenic Fungus Metabolites Militarinone C and Fumosorinone A

Militarinone C and fumosorinone A, 3-oligoenoyltetramic acids produced by insect pathogenic fungi, were synthesized for the first time. The pyrrolidine-2,4-dione ring was closed through a late-stage Dieckmann condensation of N-(β-ketoacyl) derivatives of tyrosine, obtained by its acylation with either thioesters or Meldrum's acid derivatives bearing the all-trans-polyene side chain. The latter was built up from (S)-citronellol via an Evans methylation and Wittig or HWE olefinations.

Stereoisomeric indole compounds, process for the preparation of the same, and use thereof

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