97899-30-4

Basic information

• Product Name: (3-methyl-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate
• Synonyms: (3-methyl-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate
• CAS NO: 97899-30-4
• Molecular Weight: 285.321
• Mol File: 97899-30-4.mol
• Article Data: 3

Chemical Properties

• CAS DataBase Reference: (3-methyl-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate(CAS DataBase Reference)
• NIST Chemistry Reference: (3-methyl-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate(97899-30-4)
• EPA Substance Registry System: (3-methyl-2-oxooxazolidin-5-yl)methyl 4-methylbenzenesulfonate(97899-30-4)

Safety Data

• Hazardous Substances Data: 97899-30-4(Hazardous Substances Data)

Upstream product

• 27126-76-7 [hydroxy(tosyloxy)iodo]benzene 
• 104-15-4 toluene-4-sulfonic acid 
• 1315020-11-1 5‐(hydroxymethyl)‐3‐methyl‐1,3‐oxazolidin‐2‐one 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 637343-93-2 N-methil-5-aminomethyl-2-oxazolidinone 

Relevant articles and documents

Synthesis of Oxazolidinones by a Hypervalent Iodine Mediated Cyclization of N-Allylcarbamates

The preparation of oxazolidinones by the hypervalent iodine mediated cyclization of allylcarbamates is described. A versatile range of substrates can be converted into substituted oxazolidinones primed for further transformations. Derivatization of the products at both ends is demonstrated. A preliminary attempt at the enantioselective formation of an oxazolidinone using a chiral iodane is also presented. (Figure presented.).

2-azacycloalkylthiopenem derivatives

Certain 2-azacycloalkylthio-2-penem-3-carboxylic acid compounds are useful as antibacterials for treating mammals and have the formula STR1 or a pharmaceutically acceptable salt thereof, wherein: R is STR2 A is alkylene having 2-4 carbon atoms, alkylene h