1639453-20-5

Basic information

• Product Name: 2,6-di(tert-butyl)-4-(4-fluorophenyl)-6H-[1,3,5]oxathiazine S,S-dioxide
• Synonyms: 2,6-di(tert-butyl)-4-(4-fluorophenyl)-6H-[1,3,5]oxathiazine S,S-dioxide
• CAS NO: 1639453-20-5
• Molecular Weight: 341.447
• Mol File: 1639453-20-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,6-di(tert-butyl)-4-(4-fluorophenyl)-6H-[1,3,5]oxathiazine S,S-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 2,6-di(tert-butyl)-4-(4-fluorophenyl)-6H-[1,3,5]oxathiazine S,S-dioxide(1639453-20-5)
• EPA Substance Registry System: 2,6-di(tert-butyl)-4-(4-fluorophenyl)-6H-[1,3,5]oxathiazine S,S-dioxide(1639453-20-5)

Safety Data

• Hazardous Substances Data: 1639453-20-5(Hazardous Substances Data)

Upstream product

• 756841-25-5 2,6-di(tert-butyl)-4-((p-fluoro)phenyl)-6H-1,3,5-oxathiazine 

Downstream Products

• 824-75-9 p-fluorobenzamide 

Relevant articles and documents

Synthesis, characterization, and reactivity of novel 6H-1,3,5-oxathiazine S,S-dioxides

A series of novel 6H-1,3,5-oxathiazine S,S-dioxides were synthesized by the m-CPBA oxidation (2.2 equiv) of 6H-1,3,5-oxathizines. The synthetic utilities of the newly synthesized cyclic sulfones were investigated. In a thermal condition, compounds 6H-1,3,5-oxathiazine S,S-dioxides were found relatively stable, but Lewis acid-induced thermal reaction afforded the corresponding amides. The plausible pathway to amides from 6H-1,3,5-oxathiazine S,S-dioxides was also discussed in this account.