6100-74-9
6100-74-9
Chemical Structure
3-Hydroxy-4-methoxyacetophenone
Synonym(s): Acetoisovanillone; Isoacetovanillone
- CAS No.: 6100-74-9
- Formula:C9H10O3
- Molecular Weight:166.18
IUPAC Name: 1-(3-hydroxy-4-methoxyphenyl)ethan-1-one
InChIKey: YLTGFGDODHXMFB-UHFFFAOYSA-N
SMILES: CC(C1=CC=C(OC)C(O)=C1)=O
Biological Activity: 3-Hydroxy-4-methoxyacetophenone (Acetoisovanillone; Isoacetovanillone) is an acetophenone derivative that can be isolated from the bulbs of Crinum macowanii (Amaryllidaceae). 3-Hydroxy-4-methoxyacetophenone is the phenolic acetophenone product generated from the TiO2-photocatalyzed oxidation of 3,4-dimethoxyacetophenone[1][2].
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3-Hydroxy-4-methoxyacetophenone | 98.72% | 3-Hydroxy-4-methoxyacetophenone (Acetoisovanillone; Isoacetovanillone) is an acetophenone derivative that can be isolated from the bulbs of Crinum macowanii (Amaryllidaceae). 3-Hydroxy-4-methoxyacetophenone is the phenolic acetophenone product generated from the TiO2-photocatalyzed oxidation of 3,4-dimethoxyacetophenone. | ||||||||||||||||||||
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3-Hydroxy-4-methoxyacetophenone (Standard) | ≥98% | 3-Hydroxy-4-methoxyacetophenone (Acetoisovanillone; Isoacetovanillone) (Standard) is the analytical standard of 3-Hydroxy-4-methoxyacetophenone (HY-W002484). This product is intended for research and analytical applications. 3-Hydroxy-4-methoxyacetophenone (Acetoisovanillone; Isoacetovanillone) is an acetophenone derivative that can be isolated from the bulbs of Crinum macowanii (Amaryllidaceae). 3-Hydroxy-4-methoxyacetophenone is the phenolic acetophenone product generated from the TiO2-photocatalyzed oxidation of 3,4-dimethoxyacetophenone. | ||||||||||||||||||||
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References
- [1]. Kouama M F, Tozea F A A, Wansia J D, et al. A new epi-lycorine from Crinum macowanii Baker (Amaryllidaceae)[J]. Sci Technol Dév, 2014, 16: 33-7.
- [2]. Antunes C S A, Bietti M, Salamone M, et al. Early stages in the TiO2-photocatalyzed degradation of simple phenolic and non-phenolic lignin model compounds[J]. Journal of Photochemistry and Photobiology A: Chemistry, 2004, 163(3): 453-462.
