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CAS 61775-19-7

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(2S)-7-hydroxy-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydro-4H-chromen-4-one

Description:
(2S)-7-hydroxy-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydro-4H-chromen-4-one, with the CAS number 61775-19-7, is a flavonoid compound characterized by its chromone backbone. This substance features multiple functional groups, including hydroxyl (-OH) and methoxy (-OCH3) groups, which contribute to its potential biological activities. The presence of the 4-hydroxyphenyl moiety suggests that it may exhibit antioxidant properties, as phenolic compounds are known for their ability to scavenge free radicals. The stereochemistry indicated by the (2S) configuration implies specific spatial arrangements that can influence the compound's reactivity and interaction with biological targets. Flavonoids like this compound are often studied for their pharmacological effects, including anti-inflammatory, antimicrobial, and anticancer activities. Additionally, the methoxy group can enhance lipophilicity, potentially affecting the compound's bioavailability and distribution in biological systems. Overall, this compound represents a class of natural products with significant interest in medicinal chemistry and pharmacology.
Formula:C16H14O5
InChI:InChI=1/C16H14O5/c1-20-14-6-11(18)7-15-16(14)12(19)8-13(21-15)9-2-4-10(17)5-3-9/h2-7,13,17-18H,8H2,1H3/t13-/m0/s1
Synonyms:
  • 4H-1-benzopyran-4-one, 2,3-dihydro-7-hydroxy-2-(4-hydroxyphenyl)-5-methoxy-, (2S)-
  • 5-O-Methylnaringenin
  • Naringenin 5-O-methyl ether
  • 7,4′-Dihydroxy-5-methoxyflavanone
  • (S)-7-Hydroxy-2-(4-hydroxyphenyl)-5-MethoxychroMan-4-one
  • 5-O-Methylnaringenin >=95% (LC/MS-ELSD)
  • (2S)-7-hydroxy-2-(4-hydroxyphenyl)-5-methoxy-2,3-dihydrochromen-4-one
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