3,5-Dihydroxyacetophenone

3,5-Dihydroxyacetophenone
  • CAS No.:51863-60-6
Other grades of this product :
3,5-Dihydroxyacetophenone Basic information
Product Name:3,5-Dihydroxyacetophenone
Synonyms:3',5'-DIHYDROXYACETOPHENONE;3,5-DIHYDROXYACETOPHENONE;3,5-DIHYDROXYACETOPHENONE MONOHYDRATE;1-(3,5-dihydroxyphenyl)-ethanone;5-ACETYLRESORCINOL;3,5-Dihydroxyacetophemone;ETHANONE, 1-(3,5-DIHYDROXYPHENYL)-;1-(3,5-dihydroxyphenyl)ethan-1-one
CAS:51863-60-6
MF:C8H8O3
MW:152.15
EINECS:257-480-1
Product Categories:Building Blocks for Dendrimers;Functional Materials;FINE Chemical & INTERMEDIATES;Alcohols;Monomers;Polymer Science;Aromatic Acetophenones & Derivatives (substituted);bc0001
Mol File:51863-60-6.mol
3,5-Dihydroxyacetophenone Chemical Properties
Melting point 145-146 °C(lit.)
Boiling point 234.6°C (rough estimate)
density 1.2143 (rough estimate)
refractive index 1.4447 (estimate)
storage temp. Inert atmosphere,Room Temperature
solubility DMSO (Slightly), Methanol (Slightly)
pka8.63±0.10(Predicted)
form Powder
color Off-white to brown
BRN 1936502
InChIKeyWQXWIKCZNIGMAP-UHFFFAOYSA-N
CAS DataBase Reference51863-60-6(CAS DataBase Reference)
Safety Information
Hazard Codes Xi
Risk Statements 36/37/38
Safety Statements 26-37/39-36
WGK Germany 3
HS Code 29145090
MSDS Information
ProviderLanguage
1-(3,5-Dihydroxyphenyl)-ethanone English
SigmaAldrich English
ACROS English
ALFA English
3,5-Dihydroxyacetophenone Usage And Synthesis
Chemical Propertieswhite to light yellow crystal powder
Uses3',5'-Dihydroxyacetophenone is a dihydroxy derivative of acetophenone. 3',5'-Dihydroxyacetophenone shows inhibitory activity towards plant germination and growth as well as some antitumor activity.
Uses3'',5''-Dihydroxyacetophenone is a dihydroxy derivative of acetophenone. 3'',5''-Dihydroxyacetophenone shows inhibitory activity towards plant germination and growth as well as some antitumor activity.
PreparationPreparation from 3,5-dimethoxyacetophenone (SM) by demethylation with aluminium chloride in refluxing chlorobenzene (71%) The starting material (SM) was prepared by a three-step procedure from 3,5-dimethoxy-benzoic acid.

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