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Lovastatin Diol Lactone 4-tert-Butyldimethylsilyl Ether_Molecular_structure_CAS_79902-31-1)
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Lovastatin Diol Lactone 4-tert-Butyldimethylsilyl Ether

Catalog No. L472240 Name Toronto Research Chemicals
CAS Number 79902-31-1 Website http://www.trc-canada.com
M. F. C25H42O4Si Telephone +1 (416) 665-9696
M. W. 434.68408 Fax +1 (416) 665-4439
Purity Email info@trc-canada.com
Storage Chembase ID: 172418

SYNONYMS

IUPAC name
(4R,6R)-6-{2-[(1S,2S,6R,8S,8aR)-8-hydroxy-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-[(tert-butyldimethylsilyl)oxy]oxan-2-one
IUPAC Traditional name
(4R,6R)-6-{2-[(1S,2S,6R,8S,8aR)-8-hydroxy-2,6-dimethyl-1,2,6,7,8,8a-hexahydronaphthalen-1-yl]ethyl}-4-[(tert-butyldimethylsilyl)oxy]oxan-2-one
Synonyms
(4R,6R)-4-[[(1,1-Dimethylethyl)dimethylsilyl]oxy]-6-[2-[(1S,2S,6R,8S,8aR)-1,2,6,7,8,8a-hexahydro-8-hydroxy-2,6-dimethyl-1-naphthalenyl]ethyl]tetrahydro-2H-pyran-2-one

DATABASE IDS

CAS Number 79902-31-1

PROPERTIES

Certificate of Analysis Download
Apperance White Solid
Solubility Dichloromethane
Solubility DMF
Solubility DMSO
Solubility Ether
Solubility Ethyl Acetate
Solubility Methanol
MSDS Link Download

DETAILS

Description (English)
An intermediate used for synthesis of Simvastatin precursor (H941625).

REFERENCES

  • Hoffman, W., et al.: J. Med. Chem., 29, 849 (1986)
  • Jacobsen, W., et al.: Drug Metab. Dispos., 27, 173 (1986)
  • Igel, M., et al.: Eur. J. Clin. Pharmacol., 57, 357 (1986)