Dibenzo[a,c]cyclooctene, specifically the compound with the designation 5,6,7,8-tetrahydro-1,2,3,10,11,12-hexamethoxy-6-methyl-7-methylene-, (6S,12aS)-, is a complex organic molecule characterized by its polycyclic structure, which includes a bicyclic framework derived from cyclooctene fused with two benzene rings. This compound features multiple methoxy groups, which are methanol-derived substituents that enhance its solubility and reactivity. The presence of methyl and methylene groups contributes to its structural diversity and potential biological activity. The stereochemistry indicated by the (6S,12aS) notation suggests specific spatial arrangements of atoms, which can significantly influence the compound's chemical behavior and interactions. As a chemical entity, it may exhibit unique properties such as specific reactivity patterns, potential applications in organic synthesis, or biological activity, although detailed studies would be necessary to elucidate these aspects fully. Its CAS number, 135095-47-5, allows for precise identification in chemical databases and literature.

Dibenzo[a,c]cyclooctene, 5,6,7,8-tetrahydro-1,2,3,10,11,12-hexamethoxy-6-methyl-7-methylene-, (6S,12aS)- (9CI)

135095-47-5: Dibenzo[a,c]cyclooctene, specifically the compound with the designation 5,6,7,8-tetrahydro-1,2,3,10,11,12-hexamethoxy-6-methyl-7-methylene-, (6S,12aS)-, is a complex organic molecule characterized by its polycyclic structure, which includes a bicyclic framework derived from cyclooctene fused with two benzene rings. This compound features multiple methoxy groups, which are methanol-derived substituents that enhance its solubility and reactivity. The presence of methyl and methylene groups contributes to its structural diversity and potential biological activity. The stereochemistry indicated by the (6S,12aS) notation suggests specific spatial arrangements of atoms, which can significantly influence the compound's chemical behavior and interactions. As a chemical entity, it may exhibit unique properties such as specific reactivity patterns, potential applications in organic synthesis, or biological activity, although detailed studies would be necessary to elucidate these aspects fully. Its CAS number, 135095-47-5, allows for precise identification in chemical databases and literature.

<p>7(18)-Dehydroschisandro A (7(18)-Dehydro Schisandrol A) is a lignan compound with biphenyl ring and octene-type structure, isolated from Schisandra.</p>

CAS 135095-47-5

Dibenzo[a,c]cyclooctene, 5,6,7,8-tetrahydro-1,2,3,10,11,12-hexamethoxy-6-methyl-7-methylene-, (6S,12aS)- (9CI)

7(18)-Dehydroschisandro A

Ref: TM-T83258

7(18)-Dehydroschisandro A

Ref: 54-BUP21164