5981-19-1

Basic information

• Product Name: 1,2-Oxathiolane, 5-undecyl-, 2,2-dioxide
• CAS NO: 5981-19-1
• Molecular Formula: C14H28O3S
• Mol File: 5981-19-1.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 1,2-Oxathiolane, 5-undecyl-, 2,2-dioxide(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2-Oxathiolane, 5-undecyl-, 2,2-dioxide(5981-19-1)
• EPA Substance Registry System: 1,2-Oxathiolane, 5-undecyl-, 2,2-dioxide(5981-19-1)

Safety Data

• Hazardous Substances Data: 5981-19-1(Hazardous Substances Data)

Upstream product

• 1120-36-1 1-tetradecene 

Downstream Products

• 6994-45-2 sodium n-tetradecane-1-sulphonate 
• 13513-45-6 Na-Tetradec-2-ensulfonat 
• 82099-53-4 Na-3-Ethyl-tetradecansulfonat 
• 1653-32-3 3-tetradecanol 
• 75732-56-8 1-mercapto-3-tetradecanol 
• 75732-47-7 (2,2-Dioxo-5-undecyl-2λ⁶-[1,2]oxathiolan-3-yl)-phenyl-methanol 
• 75732-60-4 1-phenyl-1,5-pentadecanediol 
• 75732-61-5 2-mercapto-1-phenyl-1,4-pentadecanediol 
• 75732-59-1 1-phenyl-4-pentadecanol 

Relevant articles and documents

Lithium aluminum hydride-aluminum hydride reduction of sultones

Lithium aluminum hydride-aluminum hydride reduction of secondary and tertiary (C-O) substituted γ-sultones or α-alkyl-β'-hydroxy γ-sultones yields mercapto alcohols and mercapto diols, respectively, in fair to good yield.These products result from S-O cleavage of the sultone ring.Primary sultones and α-dialkyl-β'-hydroxy γ-sultones give predominantly C-O cleavage to form sulfonic acid derivatives. β-Sultones are much less reactive toward the mixed hydride, and refluxing in dioxane is required for their reduction.