876-02-8

4'-Hydroxy-3'-methylacetophenone Chemical Structure
876-02-8

Chemical Structure

4'-Hydroxy-3'-methylacetophenone

  • CAS No.: 876-02-8
  • Formula:C9H10O2
  • Molecular Weight:150.18

IUPAC Name: 1-(4-hydroxy-3-methylphenyl)ethan-1-one

InChIKey: LXBHHIZIQVZGFN-UHFFFAOYSA-N

SMILES: CC(C1=CC=C(O)C(C)=C1)=O

Biological Activity: 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[1][2].

Cat. No. Product Name Purity Description Pricing
HY-W001663
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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HY-W001663R
4'-Hydroxy-3'-methylacetophenone (Standard) ≥98% 4'-Hydroxy-3'-methylacetophenone (Standard) is an analytical standard of 4'-Hydroxy-3'-methylacetophenone (HY-W001663). This product is intended for research and analytical applications. 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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References