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9-PHENYLXANTHEN-9-OL

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9-PHENYLXANTHEN-9-OL Basic information

Product Name:
9-PHENYLXANTHEN-9-OL
Synonyms:
  • LABOTEST-BB LT00159727
  • 9-PHENYL-9-XANTHENOL
  • 9-PHENYLXANTHEN-9-OL
  • 9-PHENYL-9H-XANTHEN-9-OL
  • 9-Phenylxanthydrol
  • 9-Phenylxanthen-9-ol,98%
  • 9-Phenylxanthen-9-Ol 9-Phenyl-9-Xanthenol
  • St5308451
CAS:
596-38-3
MF:
C19H14O2
MW:
274.31
EINECS:
209-882-3
Product Categories:
  • Heterocyclic Compounds
  • Fused Ring Systems
  • Heterocyclic Building Blocks
  • O-Containing
  • Others
Mol File:
596-38-3.mol
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9-PHENYLXANTHEN-9-OL Chemical Properties

Melting point:
158-161 °C(lit.)
Boiling point:
377.3°C (rough estimate)
Density 
1.1160 (rough estimate)
refractive index 
1.5510 (estimate)
form 
powder to crystal
pka
12.76±0.20(Predicted)
color 
White to Almost white
CAS DataBase Reference
596-38-3(CAS DataBase Reference)
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Safety Information

Safety Statements 
22-24/25
WGK Germany 
3
8
HS Code 
2932.99.7000

MSDS

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9-PHENYLXANTHEN-9-OL Usage And Synthesis

Chemical Properties

WHITE TO PALE YELLOW CRYSTALS OR CRYST. POWDER

Uses

Antioxidant agent-15 (Compound 4) is a potent antioxidant inhibition activity, with the IC50 of 15.44 nM. Antioxidant agent-15 inhibits tumor cell growth in Hela, Hep G2 and Caco-2 cells, with the IC50 of 395.26, 400.4 and 24.6 nM, respectively[1].

Purification Methods

Dissolve hydroxypixyl in AcOH and add H2O whereby it separates as colourless prisms. It is slightly soluble in CHCl3, soluble in *C6H6 but insoluble in pet ether. It sublimes on heating. UV in H2SO4: 450nm max ( 5620) and 370nm ( 24,900) and the HClO4 salt in CHCl3 has 450 ( 404) and 375nm ( 2420). max [Sharp J Chem Soc 2558 1958, Bünzly & Decker Chem Ber 37 2983 1904, Chattopadhyaya & Reece J Chem Soc, Chem Commun 639 1978, Gomberg & Cone Justus Liebigs Ann Chem 370 142 1909, Beilstein 17 I 80, 17 II 161, 17 III/IV 1704, 17/4 V 675.]

References

[1] Abualhasan M, et al. Biological Evaluation of Xanthene and Thioxanthene Derivatives as Antioxidant, Anticancer, and COX Inhibitors. ACS Omega. 2023;8(41):38597-38606. DOI:10.1021/acsomega.3c05695

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