2',4'-Dihydroxyacetophenone (Standard)
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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- Pureté: 98%
- CAS No.: 89-84-9
- Formule: C8H8O3
- Masse moléculaire:152.15
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Stockage:
Please store the product under the recommended conditions in the Certificate of Analysis.
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Product Information
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Chemical Information
- Pureté et documentation
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Help & FAQs
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HY-Y0694
2',4'-Dihydroxyacetophenone -
HY-N1775
3',4'-Dihydroxyacetophenone -
HY-W001174
2,5-Dihydroxyacetophenone -
HY-Y0106
2,6-Dihydroxyacetophenone -
HY-N0088
Apocynin -
HY-N1775R
3',4'-Dihydroxyacetophenone (Standard) -
HY-W001174R
2,5-Dihydroxyacetophenone (Standard) -
HY-Y0106R
2,6-Dihydroxyacetophenone (Standard) -
HY-W009849
2-Aminobenzophenone -
HY-W016168R
2-Chloro-1-(3,4-dihydroxyphenyl)ethanone (Standard) -
HY-33040
2,2',4'-Trichloroacetophenone -
HY-N0088R
Apocynin (Standard)
Product Information
Information
Application
The compound is the grade of analytical standard, which is the reference standard supplied assay. It is commonly used in qualitative, quantitative and methodological research experiments in HPLC, GC and MS.
Chemical Information
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CAS No. 89-84-9
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Masse moléculaire 152.15
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Formule C8H8O3
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SMILES
CC(C1=CC=C(O)C=C1O)=O
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Synonyms
Resacetophenone (Standard); 1-(2,4-Dihydroxyphenyl)ethanone (Standard)
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Structure Classification
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Initial Source
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Livraison
Room temperature in continental US; may vary elsewhere.
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Stockage
Please store the product under the recommended conditions in the Certificate of Analysis.
Pureté et documentation
Références
[1]. Li XJ, et al. Bioactive metabolites from biotransformation of paeonol by the white-rot basidiomycete Coriolus versicolor. Nat Prod Commun. 2011 Aug;6(8):1129-30. [Content Brief]
[2]. Baughman RG, et al. 2,4-Dinitrophenylhydrazones of 2,4-dihydroxybenzaldehyde, 2,4-dihydroxyacetophenone and 2,4-dihydroxybenzophenone. Acta Crystallogr C. 2004 Feb;60(Pt 2):o103-6. [Content Brief]
[3]. Frank A, et al. Regioselective alkylation of 2,4-dihydroxybenzyaldehydes and 2,4-dihydroxyacetophenones. Tetrahedron Lett. 2022 Apr 13;95:153755. [Content Brief]
[4]. Mutoh M, et al., Suppression by flavonoids of cyclooxygenase-2 promoter-dependent transcriptional activity in colon cancer cells: structure-activity relationship. Jpn J Cancer Res. 2000 Jul;91(7):686-91. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)
2',4'-Dihydroxyacetophenone (Standard) Related Classifications
HY-Y0694R Related Classifications
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