5211-17-6

Basic information

• Product Name: Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester
• Synonyms: Carbonodithioic acid O-(5α-cholestan-3β-yl) S-methyl ester;Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester
• CAS NO: 5211-17-6
• Molecular Formula: C₂₉H₅₀OS₂
• Molecular Weight: 478.8367
• Mol File: 5211-17-6.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 542.6±17.0 °C(Predicted)
• Appearance: /
• Density: 1.04±0.1 g/cm3(Predicted)
• CAS DataBase Reference: Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester(5211-17-6)
• EPA Substance Registry System: Dithiocarbonic acid O-(5α-cholestan-3β-yl) S-methyl ester(5211-17-6)

Safety Data

• Hazardous Substances Data: 5211-17-6(Hazardous Substances Data)

Upstream product

• 80-97-7 Cholestanol 
• 74-88-4 methyl iodide 
• 75-15-0 carbon disulfide 
• 98569-97-2 S-isopropyl-O-3β-cholestanyldithiocarbonate 
• 70242-69-2 S-benzyl xanthate de cholestanyle-3β 
• 84551-49-5 N,N-dimethyl thiocarbamate de cholestanyle-3β 
• 23405-64-3 O-methyl carbonate de cholestanyle-3β 
• 80-97-7 3-β-cholestanol 

Downstream Products

• 1666-13-3 diphenyl diselenide 
• 68587-25-7 O-5α-cholestan-3β-yl S-methyl thiocarbonate 
• 104933-78-0 3β-cholestanyloxy-triphenylmethyl-azothioformate 
• 481-20-9 (10S,13R,17R)-17-(1,5-Dimethyl-hexyl)-10,13-dimethyl-hexadecahydro-cyclopenta[a]phenanthrene 
• 481-21-0 cholestane 
• 98569-96-1 3β-cholestanyloxy methane thiol 
• 17669-94-2 cholestane-3β-thiol 
• 5847-30-3 3α-chloro-5α-cholestane 

Relevant articles and documents

13C NMR spectral assignment of five epimeric 3α- versus 3β-functionalized cholestane pairs

13C NMR chemical shift assignments of five α- and β-epimeric pairs of cholestanes functionalized at C-3 are presented. Empirical increment estimations proved to be a valuable tool for the unequivocal structural elucidation when compared with th

Reduction et photoreduction de derives de l'acide carbonique influence de l'hexamethylphosphorotriamide

Photoreduction and reduction of carbonic acid derivatives in HMPT have been compared.The highest yield of alkane was obtained from N,N-dimethylthiocarbamates either by the photochemical method or by reduction with a dissolved metal.Competitive reactions have been characterized: - during the photoreduction not only the alkane but products of a photo-Fries rearrangement and products of a homolytic cleavage were detected; - basic reactions can compete with the reduction of carbonic acid derivatives by sodium in HMPT.