Assay
97%
refractive index
n20/D 1.565 (lit.)
bp
245 °C (lit.)
density
1.08 g/mL at 25 °C (lit.)
SMILES string
Cc1ccc(C(C)=O)c(O)c1
InChI
1S/C9H10O2/c1-6-3-4-8(7(2)10)9(11)5-6/h3-5,11H,1-2H3
InChI key
LYKDOWJROLHYOT-UHFFFAOYSA-N
General description
2′-Hydroxy-4′-methylacetophenone may be used in the preparation of 4′-methyl-2′-[(p-tolylsulfonyl)oxy]acetophenone.
2′-Hydroxy-4′-methylacetophenone, also known as 1-(2-hydroxy-4-methylphenyl)ethanone can be synthesized by the Fries rearrangement of m-tolyl acetate in the presence of zirconium tetrachloride. The results from the toxicity studies on mite species suggest that 2′-hydroxy-4′-methylacetophenone possesses acaricidal property.
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
WGK
WGK 3
Flash Point(F)
230.0 °F
Flash Point(C)
110 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Journal of agricultural and food chemistry, 60(14), 3606-3611 (2012-03-21)
The acaricidal activities of 2'-hydroxy-4'-methylacetophenone derived from Angelica koreana roots and its derivatives against Dermatophagoides farinae, Dermatophagoides pteronyssinus, and Tyrophagus putrescentiae were examined by vapor phase and contact toxicity bioassays. In the vapor phase toxicity bioassay, 2'-methylacetophenone (1.25 μg/cm(2)) was
Zirconium tetrachloride as a mediator for ambient temperature ortho-fries rearrangements.
Tetrahedron, 37(42), 7659-7660 (1996)
4'-Hydroxy-3-methoxyflavones with potent antipicornavirus activity.
Journal of Medicinal Chemistry, 34(2), 736-746 (1991)
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