Benzenepropanoic acid, a-hydroxy-, 6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-ylester, [2aR-[2aa,4b,4ab,6b,9a(S*),11a,12a,12aa,12ba]]- (9CI) is a complex organic compound with a molecular formula of C36H44O10. It is a derivative of benzenepropanoic acid, featuring a hydroxyl group, multiple acetyloxy and benzoyloxy groups, and a decahydro-cyclodeca[3,4]benz[1,2-b]oxet-9-ylester structure. Benzenepropanoic acid, a-hydroxy-,6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-ylester, [2aR-[2aa,4b,4ab,6b,9a(S*),11a,12a,12aa,12ba]]- (9CI) is characterized by its chiral center at the 2a position, with a specific stereochemistry denoted by the R-enantiomer. It is a highly functionalized molecule with potential applications in pharmaceuticals or chemical research, given its intricate structure and multiple reactive sites.
The CAS Registry Mumber 131896-66-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,1,8,9 and 6 respectively; the second part has 2 digits, 6 and 6 respectively. Calculate Digit Verification of CAS Registry Number 131896-66: (8*1)+(7*3)+(6*1)+(5*8)+(4*9)+(3*6)+(2*6)+(1*6)=147 147 % 10 = 7 So 131896-66-7 is a valid CAS Registry Number.
131896-66-7SDS
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According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition
Version: 1.0
Creation Date: Aug 14, 2017
Revision Date: Aug 14, 2017
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baccatin III 13-(S-3-phenyllactate)
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For industry use only.
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131896-66-7Relevant academic research and scientific papers
Biologically Active Taxol Analogues with Deleted A-Ring Side Chain Substituents and Variable C-2' Configurations
Swindell, Charles S.,Krauss, Nancy E.,Horwitz, Susan B.,Ringel, Israel
, p. 1176 - 1184 (2007/10/02)
Taxol (1), a potent inhibitor of cell replication, enhances the assembly of tubulin into stable microtubules and promotes the formation of microtubule bundles in cells.In addition to its unique mechanism of action, taxol exhibits unusual promise as an ant
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Get Best Price for131896-66-7Benzenepropanoic acid, a-hydroxy-,6,12b-bis(acetyloxy)-12-(benzoyloxy)-2a,3,4,4a,5,6,9,10,11,12,12a,12b-dodecahydro-4,11-dihydroxy-4a,8,13,13-tetramethyl-5-oxo-7,11-methano-1H-cyclodeca[3,4]benz[1,2-b]oxet-9-ylester, [2aR-[2aa,4b,4ab,6b,9a(S*),11a,12a,12aa,12ba]]- (9CI)
