853193-64-3

Basic information

• Product Name: Toluene-4-sulfonic acid 2-((S)-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl ester
• Synonyms: Toluene-4-sulfonic acid 2-((S)-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl ester
• CAS NO: 853193-64-3
• Molecular Weight: 314.403
• Mol File: 853193-64-3.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Toluene-4-sulfonic acid 2-((S)-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Toluene-4-sulfonic acid 2-((S)-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl ester(853193-64-3)
• EPA Substance Registry System: Toluene-4-sulfonic acid 2-((S)-2,2-dimethyl-[1,3]dioxan-4-yl)-ethyl ester(853193-64-3)

Safety Data

• Hazardous Substances Data: 853193-64-3(Hazardous Substances Data)

Upstream product

• 81132-13-0 (S)-5-phenylmethoxypentane-1,3-diol 
• 632339-24-3 (R)-4-(2-Benzyloxy-ethyl)-2,2-dimethyl-[1,3]dioxane 
• 98-59-9 p-toluenesulfonyl chloride 
• 185553-79-1 (R)-2-<2,2-dimethyl-1,3-dioxan-4-yl>ethan-1-ol 

Downstream Products

• 78366-44-6 (+)-dihydrocompactin 
• 853193-72-3 (S)-2-Methyl-butyric acid (1S,4aR,7S,8S,8aS)-8-[(R)-3-(2-bromo-acetoxy)-5-trityloxy-pentyl]-7-methyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-1-yl ester 
• 853193-46-1 Bromo-acetic acid (R)-1-[2-((1S,2S,4aR,8S,8aS)-8-hydroxy-2-methyl-1,2,4a,5,6,7,8,8a-octahydro-naphthalen-1-yl)-ethyl]-3-trityloxy-propyl ester 
• 853193-71-2 (1S,4aR,7S,8S,8aS)-8-((R)-3-Hydroxy-5-trityloxy-pentyl)-7-methyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-1-ol 
• 853193-70-1 (4aR,7S,8S,8aS)-8-((R)-3-Hydroxy-5-trityloxy-pentyl)-7-methyl-3,4,4a,7,8,8a-hexahydro-2H-naphthalen-1-one 
• 853193-73-4 (S)-2-Methyl-butyric acid (1S,4aR,7S,8S,8aS)-8-[(R)-3-(2-bromo-acetoxy)-5-hydroxy-pentyl]-7-methyl-1,2,3,4,4a,7,8,8a-octahydro-naphthalen-1-yl ester 

Relevant articles and documents

Remote asymmetric induction in an intramolecular ionic Diels-Alder reaction: Application to the total synthesis of (+)-dihydrocompactin

The total synthesis of (+)-dihydrocompactin via an intramolecular ionic Diels-Alder reaction that proceeds with remote stereocontrol is described. This reaction proceeds by an intermediate vinyl-oxocarbenium ion (6), the conformational constraints of whic