1373037-72-9

Basic information

• Product Name: (S)-4-benzyl-3-(2-cyclohexylacetyl)-5,5-dimethyloxazolidin-2-one
• Synonyms: (S)-4-benzyl-3-(2-cyclohexylacetyl)-5,5-dimethyloxazolidin-2-one
• CAS NO: 1373037-72-9
• Molecular Weight: 329.439
• Mol File: 1373037-72-9.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (S)-4-benzyl-3-(2-cyclohexylacetyl)-5,5-dimethyloxazolidin-2-one(CAS DataBase Reference)
• NIST Chemistry Reference: (S)-4-benzyl-3-(2-cyclohexylacetyl)-5,5-dimethyloxazolidin-2-one(1373037-72-9)
• EPA Substance Registry System: (S)-4-benzyl-3-(2-cyclohexylacetyl)-5,5-dimethyloxazolidin-2-one(1373037-72-9)

Safety Data

• Hazardous Substances Data: 1373037-72-9(Hazardous Substances Data)

Upstream product

• 23860-35-7 cyclohexylacetic acid chloride 
• 168297-85-6 (S)-4-benzyl-5,5-dimethyloxazolidin-2-one 
• 51987-73-6 (S)-2-tert-butoxycarbonylamino-3-phenyl-propionic acid methyl ester 
• 2577-90-4 methyl (2S)-2-amino-3-phenylpropanoate 
• 5292-21-7 Cyclohexylacetic acid 
• 63-91-2 L-phenylalanine 
• 1373038-24-4 C₂₁H₂₄F₇NO₃ 
• 1207362-36-4 (S)-4-benzyl-3-hexanoyl-5,5-dimethyloxazolidin-2-one 

Downstream Products

• 1180131-05-8 (S)-2-cyclohexyl-3,3,3-trifluoropropan-1-ol 
• 1373038-23-3 C₂₀H₂₁F₃O₂ 
• 1207362-44-4 (S)-4-benzyl-3-(3,3-dimethylbutanoyl)-5,5-dimethyloxazolidin-2-one 
• 1207362-36-4 (S)-4-benzyl-3-hexanoyl-5,5-dimethyloxazolidin-2-one 
• 1312341-52-8 (S)-4-benzyl-5,5-dimethyl-N-(3-methylbutanoyl)-1,3-oxazolidin-2-one 
• 1373037-82-1 C₁₆H₁₈F₃NO₃ 
• 1373037-88-7 C₁₆H₁₈F₃NO₃ 
• 1373037-93-4 C₁₈H₁₇F₆NO₃ 
• 1373037-83-2 C₁₈H₁₈F₇NO₃ 
• 1373037-91-2 C₁₉H₁₇F₈NO₃ 
• 1373037-84-3 C₁₉H₁₈F₉NO₃ 
• 1373037-94-5 C₂₁H₁₇F₁₂NO₃ 
• 1373037-86-5 C₂₁H₁₈F₁₃NO₃ 
• 1373037-95-6 C₂₂H₁₇F₆NO₃ 

Relevant articles and documents

Asymmetric radical addition of TEMPO to titanium enolates

A mild method for a-hydroxylation of N-acyl oxazolidinones by asymmetric radical addition of the 2,2,6,6-tetramethylpiperidine N-oxy (TEMPO) radical to titanium enolates was developed. The high diastereoselectivity and broad scope of the reaction show synthetic utility for the a-hydroxylation of substrates that are not tolerant to strongly basic conditions.