CAS 61135-91-9
:(6aR,11aR)-6a,11a-Dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol
Description:
(6aR,11aR)-6a,11a-Dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol, with the CAS number 61135-91-9, is a chemical compound characterized by its complex polycyclic structure, which includes fused benzofuran and benzopyran rings. This compound features multiple hydroxyl (-OH) groups, contributing to its potential as a bioactive molecule. The stereochemistry indicated by the (6aR,11aR) designation suggests specific spatial arrangements of atoms, which can influence its biological activity and interactions. Generally, compounds of this nature may exhibit various pharmacological properties, including antioxidant, anti-inflammatory, or neuroprotective effects, although specific biological activities would depend on empirical studies. Its solubility, stability, and reactivity can vary based on environmental conditions and the presence of other substances. As with many organic compounds, safety and handling precautions are essential, particularly in laboratory settings, to mitigate any potential hazards associated with exposure or reactivity.
Formula:C15H12O4
InChI:InChI=1/C15H12O4/c16-8-2-4-11-13(5-8)18-7-12-10-3-1-9(17)6-14(10)19-15(11)12/h1-6,12,15-17H,7H2/t12-,15-/m0/s1
InChI key:InChIKey=ODMIEGVTNZNSLD-WFASDCNBSA-N
SMILES:OC=1C=C2C([C@]3([C@](C=4C(O3)=CC(O)=CC4)(CO2)[H])[H])=CC1
Synonyms:- (6aR,11aR)-6a,11a-Dihydro-6H-benzofuro[3,2-c][1]benzopyran-3,9-diol
- 3,9-Dihydroxypterocarpan
- 6H-Benzofuro(3,2-c)(1)benzopyran-3,9-diol, 6a,11a-dihydro-, (6aR-cis)-
- 6H-Benzofuro[3,2-c][1]benzopyran-3,9-diol, 6a,11a-dihydro-, (6aR,11aR)-
- Demethylmedicarpin
- (6aR,11aR)-3,9-dihydroxypterocarpan
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Found 2 products.
3,9-Dihydroxypterocarpan
CAS:3,9-Dihydroxypterocarpan and phaseollidin are all good precursors of the pterocarpan phytoalexin phaseollin.Formula:C15H12O4Purity:98%Color and Shape:SolidMolecular weight:256.257Demethylmedicarpin
CAS:<p>Demethylmedicarpin is a phytoalexin, which is a naturally occurring antimicrobial compound. It is typically derived from leguminous plants, such as alfalfa and other species within the Fabaceae family. The plant synthesizes this compound as a defense mechanism in response to pathogen attack, environmental stress, or injury.</p>Formula:C15H12O4Purity:Min. 95%Color and Shape:PowderMolecular weight:256.25 g/mol

