CAS 117229-54-6
:2-Propenoic acid,3-phenyl-,(1S,3aR,4R,5R,5aR,7S,9S,9aR,10R,11S,11aR)-5,9,10,11-tetrakis(acetyloxy)-9a-[(benzoyloxy)methyl]tetradecahydro-11a-hydroxy-1,3a-dimethyl-6-methylene-13-oxo-1,4-ethanobenzo[5,6]cycloocta[1,2-c]furan-7-ylester, (2E)-
Description:
The chemical substance known as 2-Propenoic acid, 3-phenyl-, with the CAS number 117229-54-6, is a complex organic compound characterized by its intricate molecular structure, which includes multiple functional groups and stereocenters. This compound features a propenoic acid moiety, indicating the presence of a double bond and a carboxylic acid group, which contributes to its reactivity and potential applications in polymer chemistry and organic synthesis. The presence of phenyl and various acetyloxy groups suggests that it may exhibit interesting electronic properties and could participate in various chemical reactions, such as esterification or polymerization. Additionally, the stereochemistry indicated by the specific configuration at multiple chiral centers implies that the compound may have distinct biological activities or interactions, making it of interest in medicinal chemistry. Overall, this substance exemplifies the complexity and diversity of organic compounds, with potential implications in various fields, including pharmaceuticals and materials science.
Formula:C44H48O15
Synonyms:- 2-Propenoicacid, 3-phenyl-,5,9,10,11-tetrakis(acetyloxy)-9a-[(benzoyloxy)methyl]tetradecahydro-11a-hydroxy-1,3a-dimethyl-6-methylene-13-oxo-1,4-ethanobenzo[5,6]cycloocta[1,2-c]furan-7-ylester, [1S-[1a,3ab,4a,5a,5aa,7a(E),9b,9ab,10a,11b,11ab]]-
- 1,4-Ethanobenzo[5,6]cycloocta[1,2-c]furan, 2-propenoic acid deriv.
- Taxacin
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Found 3 products.
Taxacin
CAS:Taxacin inhibits platelet aggregation (IC50: 21.9μM) and suppresses superoxide generation, responding to fMLP and AA concentration.Formula:C44H48O15Purity:98%Color and Shape:SolidMolecular weight:816.84Taxacin
CAS:<p>Taxacin is a semisynthetic antitumor agent, which is derived from the natural compound found in the bark of the Pacific yew tree, Taxus brevifolia. The source of this compound is a complex diterpenoid alkaloid that has been modified through chemical synthesis to enhance its pharmacological properties and improve its efficacy as a therapeutic agent.</p>Formula:C44H48O15Purity:Min. 95%Molecular weight:816.8 g/mol


