92206-80-9

Basic information

• Product Name: Chloro-acetic acid 4-{(5S,5aS,8aS,9R)-9-[(2S,4aS,6S,7S,8R,8aS)-7,8-bis-(2-chloro-acetoxy)-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy]-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl}-2,6-dimethoxy-phenyl ester
• CAS NO: 92206-80-9
• Molecular Weight: 818.012
• Mol File: 92206-80-9.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: Chloro-acetic acid 4-{(5S,5aS,8aS,9R)-9-[(2S,4aS,6S,7S,8R,8aS)-7,8-bis-(2-chloro-acetoxy)-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy]-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl}-2,6-dimethoxy-phenyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Chloro-acetic acid 4-{(5S,5aS,8aS,9R)-9-[(2S,4aS,6S,7S,8R,8aS)-7,8-bis-(2-chloro-acetoxy)-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy]-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl}-2,6-dimethoxy-phenyl ester(92206-80-9)
• EPA Substance Registry System: Chloro-acetic acid 4-{(5S,5aS,8aS,9R)-9-[(2S,4aS,6S,7S,8R,8aS)-7,8-bis-(2-chloro-acetoxy)-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-6-yloxy]-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl}-2,6-dimethoxy-phenyl ester(92206-80-9)

Safety Data

• Hazardous Substances Data: 92206-80-9(Hazardous Substances Data)

Upstream product

• 477-47-4 (+/-)-podophyllotoxin 
• 6559-91-7 (+/-)-4'-O-demethyl-1-epipodophyllotoxin 
• 112146-43-7 Chloro-acetic acid (2S,4aS,6S,7S,8R,8aS)-7-(2-chloro-acetoxy)-6-hydroxy-2-methyl-hexahydro-pyrano[3,2-d][1,3]dioxin-8-yl ester 
• 92206-82-1 Chloro-acetic acid 4-((5S,5aS,9R)-9-hydroxy-6-oxo-5,5a,6,8,8a,9-hexahydro-furo[3',4':6,7]naphtho[2,3-d][1,3]dioxol-5-yl)-2,6-dimethoxy-phenyl ester 
• 2280-44-6 D-Glucose 
• 92206-84-3 2,3-di-O-chloroacetyl-4:6-O-ethylidene-β-D-glucopuranose 

Relevant articles and documents

Syntheses of All Four Possible Diastereomers of Etoposide and Its Aminoglycosidic Analogues via Optical Resolution of (+/-)-Podophyllotoxin by Glycosidation with D- and L-Sugars

Syntheses of all four possible diastereomers of etoposide and its aminoglycosidic analogues have been achieved via optical resolution of (+/-)-podophyllotoxin by glycosidation with D- and L-sugars.