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CAS 78213-66-8

:

(2R,3S,3aR,4aS,4bS,6aR,7S,7dR,8S,9aR,14bS,14cR,16aS)-14b,14c,17,17-tetramethyl-2-(1-methylethenyl)-10-methylidene-3,3a,6,6a,7,8,9,9a,10,11,14,14b,14c,15,16,16a-hexadecahydro-2H,4bH-7,8-(epoxymethano)cyclobuta[5,6]benzo[1,2-e]oxireno[4',4a']chromeno[5',6':

Description:
The chemical substance with the name "(2R,3S,3aR,4aS,4bS,6aR,7S,7dR,8S,9aR,14bS,14cR,16aS)-14b,14c,17,17-tetramethyl-2-(1-methylethenyl)-10-methylidene-3,3a,6,6a,7,8,9,9a,10,11,14,14b,14c,15,16,16a-hexadecahydro-2H,4bH-7,8-(epoxymethano)cyclobuta[5,6]benzo[1,2-e]oxireno[4',4a']chromeno[5',6']" and CAS number "78213-66-8" is a complex organic compound characterized by its intricate stereochemistry and multiple functional groups. It features a polycyclic structure with several chiral centers, indicating potential for diverse biological activity. The presence of epoxide and methylene groups suggests reactivity that may be exploited in synthetic applications or biological interactions. This compound is likely to exhibit hydrophobic properties due to its extensive hydrocarbon framework, which may influence its solubility and interaction with biological membranes. Additionally, the presence of multiple methyl groups may enhance its stability and lipophilicity. Overall, this substance represents a unique class of organic molecules with potential applications in pharmaceuticals or as natural products, although specific biological activities would require further investigation.
Formula:C37H45NO6
InChI:InChI=1/C37H45NO6/c1-16(2)28-27(39)31-37(44-31)23(42-28)11-12-33(6)34(7)19(10-13-35(33,37)40)29-25-24-21(38-30(25)34)9-8-18-14-17(3)20-15-22(32(4,5)43-29)36(20,41)26(18)24/h8-9,19-20,22-23,27-29,31,38-41H,1,3,10-15H2,2,4-7H3/t19-,20+,22+,23-,27-,28+,29-,31+,33+,34+,35-,36+,37-/m0/s1
Synonyms:
  • 6-Dechloropenitrem A
  • Dechloropenitrem A
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