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CAS 61135-92-0

:

(6aS,11aS)-9-Methoxy-6H-benzofuro[3,2-c][1]benzopyran-3,6a(11aH)-diol

Description:
The chemical substance known as "(6aS,11aS)-9-Methoxy-6H-benzofuro[3,2-c][1]benzopyran-3,6a(11aH)-diol," with the CAS number 61135-92-0, is a complex organic compound characterized by its unique polycyclic structure, which includes a benzofuro and benzopyran moiety. This compound features multiple hydroxyl (-OH) groups, contributing to its potential for hydrogen bonding and solubility in polar solvents. The methoxy (-OCH3) group enhances its lipophilicity and may influence its biological activity. The stereochemistry indicated by the (6aS,11aS) configuration suggests specific spatial arrangements of atoms, which can significantly affect the compound's reactivity and interaction with biological targets. Such compounds are often studied for their potential pharmacological properties, including antioxidant and anti-inflammatory activities. Additionally, the presence of multiple aromatic rings may contribute to its stability and electronic properties, making it of interest in various fields, including medicinal chemistry and materials science. Further studies would be necessary to elucidate its specific applications and mechanisms of action.
Formula:C16H14O5
InChI:InChI=1S/C16H14O5/c1-19-10-3-5-12-14(7-10)21-15-11-4-2-9(17)6-13(11)20-8-16(12,15)18/h2-7,15,17-18H,8H2,1H3/t15-,16+/m0/s1
InChI key:InChIKey=SXKBOSYKWYQHMV-JKSUJKDBSA-N
SMILES:O[C@]12[C@](C=3C(OC1)=CC(O)=CC3)(OC=4C2=CC=C(OC)C4)[H]
Synonyms:
  • 6H-Benzofuro[3,2-c][1]benzopyran-3,6a(11aH)-diol, 9-methoxy-, (6aS,11aS)-
  • 3-Hydroxymedicarpin
  • (6aS,11aS)-9-Methoxy-6H-benzofuro[3,2-c][1]benzopyran-3,6a(11aH)-diol
  • 6H-Benzofuro[3,2-c][1]benzopyran-3,6a(11aH)-diol, 9-methoxy-, (6aS-cis)-
  • 6a-Hydroxymedicarpin
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