CAS 122537-60-4

(3S,4aS,6aS,7aR,10aS,11aS,11bR,11cR)-3-(Acetyloxy)-1,2,3,4,4a,5,6,11a,11b,11c-decahydro-4,4,8,11c-tetramethylbisoxireno[1,10a:3,4]phenanthro[3,2-b]furan-9(7aH)-one

Description:

The chemical substance with the name "(3S,4aS,6aS,7aR,10aS,11aS,11bR,11cR)-3-(Acetyloxy)-1,2,3,4,4a,5,6,11a,11b,11c-decahydro-4,4,8,11c-tetramethylbisoxireno[1,10a:3,4]phenanthro[3,2-b]furan-9(7aH)-one" and CAS number "122537-60-4" is a complex organic compound characterized by its intricate polycyclic structure and multiple stereocenters. This compound features a fused ring system, which contributes to its unique three-dimensional conformation and potential biological activity. The presence of an acetyloxy group indicates that it may participate in various chemical reactions, such as esterification or hydrolysis. Its multiple methyl groups suggest a degree of hydrophobicity, which could influence its solubility and interaction with biological membranes. The specific stereochemistry of the compound is crucial for its biological function, as it may interact with specific receptors or enzymes in a stereospecific manner. Overall, this compound's structural complexity and functional groups make it a subject of interest in fields such as medicinal chemistry and natural product synthesis.

Formula: C₂₂H₂₈O₆

InChI: InChI=1S/C22H28O6/c1-10-14-16-21(26-16)9-6-12-19(3,4)13(25-11(2)23)7-8-20(12,5)15(21)17-22(14,27-17)28-18(10)24/h12-13,15-17H,6-9H2,1-5H3/t12-,13+,15+,16-,17+,20-,21+,22+/m1/s1

InChI key: InChIKey=WDPSZJMRQVJIBN-CLAXDQGUSA-N

SMILES: C[C@]12[C@]3([C@]4([C@](O4)(C=5[C@@]6([C@]3(O6)[H])OC(=O)C5C)[H])CC[C@@]1(C(C)(C)[C@@H](OC(C)=O)CC2)[H])[H]

Synonyms:

• (3S,4aS,6aS,7aR,10aS,11aS,11bR,11cR)-3-(Acetyloxy)-1,2,3,4,4a,5,6,11a,11b,11c-decahydro-4,4,8,11c-tetramethylbisoxireno[1,10a:3,4]phenanthro[3,2-b]furan-9(7aH)-one
• Bisoxireno[1,10a:3,4]phenanthro[3,2-b]furan-9(7aH)-one,3-(acetyloxy)-1,2,3,4,4a,5,6,11a,11b,11c-decahydro-4,4,8,11c-tetramethyl-,[3S-(3a,4aa,6aR*,7ab,10aR*,11aa,11ba,11cb)]-
• Gelomulide B
• Bisoxireno[1,10a:3,4]phenanthro[3,2-b]furan-9(7aH)-one, 3-(acetyloxy)-1,2,3,4,4a,5,6,11a,11b,11c-decahydro-4,4,8,11c-tetramethyl-, (3S,4aS,6aS,7aR,10aS,11aS,11bR,11cR)-

Bisoxireno[1,10a:3,4]phenanthro[3,2-b]furan-9(7aH)-one, 3-(acetyloxy)-1,2,3,4,4a,5,6,11a,11b,11c-decahydro-4,4,8,11c-tetramethyl-, (3S,4aS,6aS,7aR,10aS,11aS,11bR,11cR)-

CAS: 122537-60-4

Formula: C₂₂H₂₈O₆

Purity: 97.5%

Color and Shape: Solid

Molecular weight: 388.4541

Ref: IN-DA0017FN

Gelomulide B

CAS: 122537-60-4

Gelomulide B is a natural product for research related to life sciences. The catalog number is TN4120 and the CAS number is 122537-60-4.

Formula: C₂₂H₂₈O₆

Purity: 98%

Color and Shape: Solid

Molecular weight: 388.46

Ref: TM-TN4120

Gelomulide B

CAS: 122537-60-4

Formula: C₂₂H₂₈O₆

Purity: 95%~99%

Molecular weight: 388.46

Ref: BP-SBP03204

(5,12,16,16-Tetramethyl-6-oxo-2,7,9-trioxahexacyclo[9.8.0.01,3.04,8.08,10.012,17]nonadec-4-en-15-yl) acetate

CAS: 122537-60-4

(5,12,16,16-Tetramethyl-6-oxo-2,7,9-trioxahexacyclo[9.8.0.01,3.04,8.08,10.012,17]nonadec-4-en-15-yl) acetate is an intricate organic compound, commonly studied within the realms of chemistry and materials science. This compound is typically synthesized through a series of organic reactions using precursors found in various natural and synthetic sources. Its mode of action involves unique structural properties that allow for interactions with multiple chemical systems.

Formula: C₂₂H₂₈O₆

Purity: Min. 95%

Molecular weight: 388.5 g/mol

Ref: 3D-XEA53760