6921-64-8
Chemical Structure
2'-Hydroxy-4'-methylacetophenone
- CAS No.: 6921-64-8
- Formula:C9H10O2
- Molecular Weight:150.18
IUPAC Name: 1-(2-hydroxy-4-methylphenyl)ethan-1-one
InChIKey: LYKDOWJROLHYOT-UHFFFAOYSA-N
SMILES: CC(C1=CC=C(C)C=C1O)=O
Biological Activity: 2'-Hydroxy-4'-methylacetophenone is an acetophenone (HY-Y0989) derivative and acaricide that can be isolated from the roots of Angelica koreana. 2'-Hydroxy-4'-methylacetophenone exhibits toxicity against mites. It serves as a starting material for the synthesis of flavonoid derivatives. 2'-Hydroxy-4'-methylacetophenone can be used in studies related to infestations of house dust mites and stored food mites[1][2].
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2'-Hydroxy-4'-methylacetophenone | 99.76% | 2'-Hydroxy-4'-methylacetophenone is an acetophenone (HY-Y0989) derivative and acaricide that can be isolated from the roots of Angelica koreana. 2'-Hydroxy-4'-methylacetophenone exhibits toxicity against mites. It serves as a starting material for the synthesis of flavonoid derivatives. 2'-Hydroxy-4'-methylacetophenone can be used in studies related to infestations of house dust mites and stored food mites. | ||||||||||||||||||||
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Similarity Score 0.99
HY-W100681R2'-Hydroxy-5'-methylacetophenone (Standard) -
Similarity Score 0.92
HY-W1527362-Methyl-5-acetylphenol -
Similarity Score 0.92
HY-W0016634'-Hydroxy-3'-methylacetophenone -
Similarity Score 0.92
HY-W0102544′-Hydroxy-2′-methylacetophenone -
Similarity Score 0.89
HY-W001174R2,5-Dihydroxyacetophenone (Standard) -
Similarity Score 0.88
HY-Y06942',4'-Dihydroxyacetophenone -
Similarity Score 0.88
HY-222251-(4-Chloro-2-hydroxyphenyl)ethan-1-one -
Similarity Score 0.88
HY-W0047135′-Chloro-2′-hydroxyacetophenone -
Similarity Score 0.88
HY-W006911Acebutolol impurity 5 -
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References
- [1]. Oh MS, et al. Acaricidal toxicity of 2'-hydroxy-4'-methylacetophenone isolated from Angelicae koreana roots and structure-activity relationships of its derivatives. J Agric Food Chem. 2012 Apr 11;60(14):3606-11. [Content Brief]
- [2]. De Meyer N, et al. 4'-Hydroxy-3-methoxyflavones with potent antipicornavirus activity. Journal of medicinal chemistry. 1991 Feb;34(2):736-46. [Content Brief]