935658-30-3

Basic information

• Product Name: (3,5-dimethoxy-phenyl)-acetic acid 3-acetoxy-5-(4-benzyl-2-oxo-oxazolidin-3-yl)-1-methyl-4-methylsulfanyl-5-oxo-pentyl ester
• Synonyms: (3,5-dimethoxy-phenyl)-acetic acid 3-acetoxy-5-(4-benzyl-2-oxo-oxazolidin-3-yl)-1-methyl-4-methylsulfanyl-5-oxo-pentyl ester
• CAS NO: 935658-30-3
• Molecular Weight: 573.664
• Mol File: 935658-30-3.mol

Chemical Properties

• CAS DataBase Reference: (3,5-dimethoxy-phenyl)-acetic acid 3-acetoxy-5-(4-benzyl-2-oxo-oxazolidin-3-yl)-1-methyl-4-methylsulfanyl-5-oxo-pentyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3,5-dimethoxy-phenyl)-acetic acid 3-acetoxy-5-(4-benzyl-2-oxo-oxazolidin-3-yl)-1-methyl-4-methylsulfanyl-5-oxo-pentyl ester(935658-30-3)
• EPA Substance Registry System: (3,5-dimethoxy-phenyl)-acetic acid 3-acetoxy-5-(4-benzyl-2-oxo-oxazolidin-3-yl)-1-methyl-4-methylsulfanyl-5-oxo-pentyl ester(935658-30-3)

Safety Data

• Hazardous Substances Data: 935658-30-3(Hazardous Substances Data)

Upstream product

• 935658-21-2 (R)-1-formylpropan-2-yl 2-(3,5-dimethoxyphenyl)acetate 
• 108-24-7 acetic anhydride 
• 190664-60-9 (4S)-3-(Methylthioacetyl)-4-benzyl-1,3-oxazolidin-2-one 
• 6512-32-9 methyl 2-(3,5-dimethoxyphenyl)acetate 
• 4670-10-4 (3,5-dimethoxyphenyl)acetic acid 
• 935658-20-1 (R)-1-(1,3-dithian-2-yl)propan-2-yl 2-(3,5-dimethoxyphenyl)acetate 

Downstream Products

• 935658-33-6 3-acetoxy-5-[(3,5-dimethoxy-phenyl)-acetoxy]-hexanoic acid 
• 935658-32-5 (3,5-dimethoxy-phenyl)-acetic acid 3-acetoxy-5-(4-benzyl-2-oxo-oxazolidin-3-yl)-1-methyl-5-oxo-pentyl ester 

Relevant articles and documents

The first asymmetric total syntheses and determination of absolute configurations of xestodecalactones B and C

The first efficient asymmetric total syntheses of xestodecalactones B and C have been accomplished in 10 steps with an overall yield of 22 and 20.2%, respectively. The key steps involve the utility of Evans oxazolidinone-mediated syn-aldol condensations to establish the C-9 configuration and the macrolide ring formation by intramolecular acylation. The absolute configurations of xestodecalactones B and C have been determined via these syntheses.