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ChemicalBook--->CAS DataBase List--->210690-85-0

210690-85-0

210690-85-0 Structure

210690-85-0 Structure
IdentificationBack Directory
[Name]

4-[(1E,3S,5Z,8R/S,10S)-3,11-Bis-{[tert-butyl(dimethyl)silyl]oxy}-2,6,10-trimethyl-undeca-1,5-dienyl]-2-methyl-1,3-thiazole
[CAS]

210690-85-0
[Synonyms]

4-[(1E,3S,5Z,10S)-3,11-Bis[[(1,1-diMethylethyl)diMethylsilyl]oxy]-2,6,10-triMethyl-1,5-undecadien-1-yl]-2-Methyl-thiazole
4-[(1E,3S,5Z,8R/S,10S)-3,11-Bis-{[tert-butyl(dimethyl)silyl]oxy}-2,6,10-trimethyl-undeca-1,5-dienyl]-2-methyl-1,3-thiazole
[Molecular Formula]

C30H57NO2SSi2
[MDL Number]

MFCD04039436
[MOL File]

210690-85-0.mol
[Molecular Weight]

552.015
Chemical PropertiesBack Directory
[Appearance]

Colourless Oil
[Boiling point ]

550.1±50.0 °C(Predicted)
[density ]

0.939±0.06 g/cm3(Predicted)
[solubility ]

Chloroform, Dichloromethane, Ethanol, Ethyl Acetate, Methanol, Toluene
[form ]

Oil
[pka]

2.73±0.10(Predicted)
[color ]

Colourless
Hazard InformationBack Directory
[Chemical Properties]

Colourless Oil
[Uses]

An intermediate in the synthesis of Epothilones. Epothilones are polyketide natural products that inhibit cancer cells by a mechanism similar to paclitaxel, and also are effective against paclitaxel-resistant tumours. Epothilone D is in phase I clinical testing of in patients with advanced solid tumours. Epothilone D is a cytotoxic macrolide that stabilises malignant cells' microtubules and arrests mitosis, a characteristic it shares with other epothilones. They bind to the same hepatic sites as does paclitaxel (Taxol) in a 1:1 stoichiometric ratio of a, b-tubulin heterodimers.
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