875-59-2
875-59-2
Chemical Structure
4′-Hydroxy-2′-methylacetophenone
- CAS No.: 875-59-2
- Formula:C9H10O2
- Molecular Weight:150.18
IUPAC Name: 1-(4-hydroxy-2-methylphenyl)ethan-1-one
InChIKey: IAMNVCJECQWBLZ-UHFFFAOYSA-N
SMILES: CC(C1=CC=C(O)C=C1C)=O
Biological Activity: 4′-Hydroxy-2′-methylacetophenone is an aroma compound in red wine, which can be isolated from the cv. Bobal grape variety. 4′-Hydroxy-2′-methylacetophenone accumulates in adipose tissues and exerts non-specific membrane effects on Tetrahymena pyriformis. 4′-Hydroxy-2′-methylacetophenone inhibits the growth of Tetrahymena pyriformis[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4′-Hydroxy-2′-methylacetophenone | 99.67% | 4′-Hydroxy-2′-methylacetophenone is an aroma compound in red wine, which can be isolated from the cv. Bobal grape variety. 4′-Hydroxy-2′-methylacetophenone accumulates in adipose tissues and exerts non-specific membrane effects on Tetrahymena pyriformis. 4′-Hydroxy-2′-methylacetophenone inhibits the growth of Tetrahymena pyriformis. | ||||||||||||||||||||
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4′-Hydroxy-2′-methylacetophenone (Standard) | ≥98% | 4′-Hydroxy-2′-methylacetophenone (Standard) is the analytical standard of 4′-Hydroxy-2′-methylacetophenone (HY-W010254). This product is intended for research and analytical applications. 4′-Hydroxy-2′-methylacetophenone, an aroma compound of red wines, is isolated from cv. Bobal grape variety. 4′-Hydroxy-2′-methylacetophenone has ciliate toxicity. 4′-Hydroxy-2′-methylacetophenone inhibits the growth of T. pyriformis, with an IC50 of 0.65 mM. | ||||||||||||||||||||
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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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2,5-Dihydroxyacetophenone | 99.95% | 2,5-Dihydroxyacetophenone, isolated from Rehmannia glutinosa, inhibits the production of inflammatory mediators in activated macrophages by blocking the ERK1/2 and NF-κB signaling pathways. | ||||||||||||||||||||
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4'-Hydroxy-3'-methylacetophenone | 99.96% | 4'-Hydroxy-3'-methylacetophenone is a phenolic volatile compound. 4'-Hydroxy-3'-methylacetophenone can be isolated from Hawaiian green coffee beans (Coffea Arabica L.). 4'-Hydroxy-3'-methylacetophenone is believed to possess potent antioxidant activity similar to that of other phenolic volatile compounds, Thymol (HY-N6810) and Eugenol (HY-N0337). 4'-Hydroxy-3'-methylacetophenone also can be used to synthesize heterocyclic compounds which have antimycobacterial activity. | ||||||||||||||||||||
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Acebutolol impurity 5 | Acebutolol impurity 5 is an impurity of Acebutolol. | |||||||||||||||||||||
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2',4'-Dimethylacetophenone (Standard) | ≥98% | 2',4'-Dimethylacetophenone (Standard) is the analytical standard of 2',4'-Dimethylacetophenone (HY-W015618). This product is intended for research and analytical applications. 2',4'-Dimethylacetophenone is an endogenous metabolite. | ||||||||||||||||||||
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Methyl 5-hydroxy-2-methylbenzoate | Methyl 5-hydroxy-2-methylbenzoate is a catalyst in biochemical reactions. | |||||||||||||||||||||
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2'-Hydroxy-5'-methylacetophenone | 99.97% | 2'-Hydroxy-5'-methylacetophenone belongs to the class of organic compounds known as alkyl-phenylketones. These are aromatic compounds containing a ketone substituted by one alkyl group, and a phenyl group. | ||||||||||||||||||||
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2-Methyl-5-acetylphenol | 2-Methyl-5-acetylphenol is a hydroxylated methylacetophenone that exists in the aerial parts of Cannabis sativa subsp. sativa. 2-Methyl-5-acetylphenol exhibits strong binding affinity to HIPK2. 2-Methyl-5-acetylphenol cannot reverse MPP+ (1-methyl-4-phenyl-pyridinium ion)-induced neuronal cytotoxicity. 2-Methyl-5-acetylphenol can be used for Parkinson's disease research. | |||||||||||||||||||||
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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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2',4'-Dihydroxyacetophenone (Standard) | ≥98% | 2',4'-Dihydroxyacetophenone (Resacetophenone) is acetophenone carrying hydroxy substituents at positions 2' and 4'. 2',4'-Dihydroxyacetophenone involves in a practical CsHCO3-mediated alkylation that efficiently provide 4-alkylated products with excellent regioselectivity, good isolated yields and a broad substrate scope. 2',4'-Dihydroxyacetophenone is a plant metabolite. | ||||||||||||||||||||
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References
- [1]. Schüürmann G, et al. Stepwise discrimination between four modes of toxic action of phenols in the Tetrahymena pyriformis assay. Chemical research in toxicology. 2003 Aug;16(8):974-87. [Content Brief]
- [2]. Gómez García‑Carpintero E, et al. Aroma characterization of red wines from cv. Bobal grape variety grown in La Mancha region. Food Research International. 2011 Jan;44(1):61‑70.
