CAS 2510-71-6
:rel-(9R,10S)-9,10-Dihydro-9,10-phenanthrenediol
Description:
Rel-(9R,10S)-9,10-Dihydro-9,10-phenanthrenediol, with the CAS number 2510-71-6, is a polycyclic aromatic compound characterized by its unique bicyclic structure derived from phenanthrene. This compound features two hydroxyl (-OH) groups located at the 9 and 10 positions of the phenanthrene framework, which contributes to its reactivity and potential biological activity. The stereochemistry indicated by the "rel-(9R,10S)" notation suggests specific spatial arrangements of the hydroxyl groups, which can influence the compound's interactions in chemical reactions and biological systems. Typically, compounds like this may exhibit properties such as solubility in organic solvents, potential antioxidant activity, and the ability to participate in hydrogen bonding due to the presence of hydroxyl groups. Its structural characteristics may also allow it to engage in various chemical transformations, making it of interest in organic synthesis and medicinal chemistry. Overall, the compound's unique structure and functional groups contribute to its potential applications in various fields, including pharmaceuticals and materials science.
Formula:C14H12O2
InChI:InChI=1/C14H12O2/c15-13-11-7-3-1-5-9(11)10-6-2-4-8-12(10)14(13)16/h1-8,13-16H/t13-,14+
InChI key:InChIKey=MFXNBQWUTDDOKE-OKILXGFUNA-N
SMILES:O[C@H]1C=2C(C=3C([C@H]1O)=CC=CC3)=CC=CC2
Synonyms:- (E)-9,10-Dihydro-9,10-phenanthrenediol
- (E)-9,10-Dihydroxy-9,10-dihydrophenanthrene
- 9,10-Dihydrophenanthrene-cis-9,10-diol
- 9,10-Phenanthrenediol, 9,10-Dihydro-
- 9,10-Phenanthrenediol, 9,10-dihydro-, (9R,10S)-rel-
- 9,10-Phenanthrenediol, 9,10-dihydro-, cis-
- Phenanthrene cis-9,10-dihydrodiol
- cis-9,10-Dihydro-9,10-phenanthrenediol
- cis-9,10-Dihydroxy-9,10-dihydrophenanthrene
- rel-(9R,10S)-9,10-Dihydro-9,10-phenanthrenediol
- 9,10-Dihydrophenanthrene-9,10-diol
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Found 1 products.
cis-9,10-Dihydroxy-9,10-dihydrophenanthrene
CAS:Controlled ProductApplications A dihydroxy metabolite of Phenanthrene with cis conformation. Produced via degradation by phenoloxidases and dioxygenases of Polyporus sp. S133.
References Hadibarata, T. et al.: J. Microb. Biotech., 21, 299 (2011); Pathak, H. et al.: Bioremed., 12, 119 (2008); Moody, J.D. et al.: App. Env. Microbiol., 67, 1476 (2001);Formula:C14H12O2Color and Shape:NeatMolecular weight:212.24
