187227-25-4

Basic information

• Product Name: (3aR,5S,7R,7aR)-5-Hydroxy-2,2-dimethyl-7-(toluene-4-sulfonyloxy)-hexahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester
• Synonyms: (3aR,5S,7R,7aR)-5-Hydroxy-2,2-dimethyl-7-(toluene-4-sulfonyloxy)-hexahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester
• CAS NO: 187227-25-4
• Molecular Weight: 400.45
• Mol File: 187227-25-4.mol
• Article Data: 2

Chemical Properties

• CAS DataBase Reference: (3aR,5S,7R,7aR)-5-Hydroxy-2,2-dimethyl-7-(toluene-4-sulfonyloxy)-hexahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: (3aR,5S,7R,7aR)-5-Hydroxy-2,2-dimethyl-7-(toluene-4-sulfonyloxy)-hexahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester(187227-25-4)
• EPA Substance Registry System: (3aR,5S,7R,7aR)-5-Hydroxy-2,2-dimethyl-7-(toluene-4-sulfonyloxy)-hexahydro-benzo[1,3]dioxole-5-carboxylic acid methyl ester(187227-25-4)

Safety Data

• Hazardous Substances Data: 187227-25-4(Hazardous Substances Data)

Upstream product

• 32384-42-2 (1S,3R,4S,5R)-3,4-O-isopropylidene-1,5-quinic lactone 
• 97373-88-1 methyl (1R,3R,4S,5R)-1,5-dihydroxy-3,4-(isopropylidenedioxy)cyclohexane-1-carboxylate 
• 98-59-9 p-toluenesulfonyl chloride 

Downstream Products

• 208720-64-3 (3R,4R,5S)-5-Azido-4-propionylamino-3-propoxy-cyclohex-1-enecarboxylic acid methyl ester 
• 208720-60-9 (3R,4R,5S)-5-Azido-4-methanesulfonylamino-3-propoxy-cyclohex-1-enecarboxylic acid methyl ester 
• 208720-57-4 C₂₃H₃₈N₄O₈ 
• 208589-19-9 (3R,4R,5S)-4-acetamido-5-(N²,N³-bis(tert-butoxycarbonyl)guanidino)-3-propoxy-1-cyclohexene-1-carboxylic acid 
• 208589-18-8 (3R,4R,5S)-4-Acetylamino-5-amino-3-propoxy-cyclohex-1-enecarboxylic acid methyl ester 

Relevant articles and documents

Influenza neuraminidase inhibitors possessing a novel hydrophobic interaction in the enzyme active site: Design, synthesis, and structural analysis of carbocyclic sialic acid analogues with potent anti-influenza activity

The design, synthesis, and in vitro evaluation of the novel carbocycles as transition-state-based inhibitors of influenza neuraminidase (NA) are described. The double bond position in the carbocyclic analogues plays an important role in NA inhibition as d