121-71-1
121-71-1
Chemical Structure
3-Hydroxyacetophenone
Synonym(s): m-Hydroxyacetophenone
- CAS No.: 121-71-1
- Formula:C8H8O2
- Molecular Weight:136.15
IUPAC Name: 1-(3-hydroxyphenyl)ethan-1-one
InChIKey: LUJMEECXHPYQOF-UHFFFAOYSA-N
SMILES: CC(C1=CC=CC(O)=C1)=O
Biological Activity: 3-Hydroxyacetophenone (m-Hydroxyacetophenone) is a hydroxy-substituted alkyl phenyl ketone and also a plant defensin in carnations. 3-Hydroxyacetophenone has antifusarium activity. In addition, 3-Hydroxyacetophenone can be used to synthesize Rivastigmine (HY-17368)[1][2][3].
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3-Hydroxyacetophenone | 99.89% | 3-Hydroxyacetophenone (m-Hydroxyacetophenone) is a hydroxy-substituted alkyl phenyl ketone and also a plant defensin in carnations. 3-Hydroxyacetophenone has antifusarium activity. In addition, 3-Hydroxyacetophenone can be used to synthesize Rivastigmine (HY-17368). | ||||||||||||||||||||
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3-Hydroxyacetophenone (Standard) | ≥98% | 3-Hydroxyacetophenone (Standard) is the analytical standard of 3-Hydroxyacetophenone (HY-Y0603). This product is intended for research and analytical applications. 3-Hydroxyacetophenone (m-Hydroxyacetophenone) is a hydroxy-substituted alkyl phenyl ketone and also a plant defensin in carnations. 3-Hydroxyacetophenone has antifusarium activity. In addition, 3-Hydroxyacetophenone can be used to synthesize Rivastigmine (HY-17368). | ||||||||||||||||||||
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Structural Analogs
-
Similarity Score 0.92
HY-Y0073R4-Hydroxyacetophenone (Standard) -
Similarity Score 0.88
HY-Y1426R2'-Hydroxyacetophenone (Standard) -
Similarity Score 0.87
HY-W0126373-Acetylaniline -
Similarity Score 0.86
HY-W004049R3-Hydroxybenzoic acid (Standard) -
Similarity Score 0.86
HY-90004Methyl 3-hydroxybenzoate -
Similarity Score 0.85
HY-W1527362-Methyl-5-acetylphenol -
Similarity Score 0.85
HY-W0102544′-Hydroxy-2′-methylacetophenone -
Similarity Score 0.85
HY-W001663R4'-Hydroxy-3'-methylacetophenone (Standard) -
Similarity Score 0.85
HY-N17753',4'-Dihydroxyacetophenone -
Explore the MedChemAI to find more analogs
References
- [1]. Katharine Moore Tibbetts, et al. Controlling dissociation of alkyl phenyl ketone radical cations in the strong-field regime through hydroxyl substitution position. J Phys Chem A. 2014 Sep 18;118(37):8170-6. [Content Brief]
- [2]. Kiwon Han, et al. Chemoenzymatic synthesis of rivastigmine via dynamic kinetic resolution as a key step. J Org Chem. 2010 May 7;75(9):3105-8. [Content Brief]
- [3]. Curir P, et al. 3-Hydroxyacetophenone in carnations is a phytoanticipin active against Fusarium oxysporum f. sp. dianthi. Phytochemistry, 1996, 41(2): 447-450.
