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| 4,6-DIACETYLRESORCINOL Basic information |
Product Name: | 4,6-DIACETYLRESORCINOL | Synonyms: | Ethanone, 1,1'-(4,6-dihydroxy-1,3-phenylene)bis-;4,6-DIACETYLRESORCINOL;AKOS 236-35;1,1'-(4,6-DIHYDROXY-1,3-PHENYLENE)BISETHANONE;1,1'-(4,6-dihydroxy-1,3-phenylene)bisethan-1-one;1-(5-ACETYL-2,4-DIHYDROXYPHENYL)ETHAN-1-ONE;RESODIACETOPHENONE;1,1'-(4,6-Dihydroxy-1,3-phenylene)bisethanone 99% | CAS: | 2161-85-5 | MF: | C10H10O4 | MW: | 194.18 | EINECS: | 218-482-8 | Product Categories: | Aromatic Acetophenones & Derivatives (substituted);Building Blocks;C10;Carbonyl Compounds;Chemical Synthesis;Ketones;Organic Building Blocks | Mol File: | 2161-85-5.mol | |
| 4,6-DIACETYLRESORCINOL Chemical Properties |
Melting point | 178-180 °C(lit.) | Boiling point | 399.9±27.0 °C(Predicted) | density | 1.300±0.06 g/cm3(Predicted) | storage temp. | Inert atmosphere,Room Temperature | pka | 7.87±0.23(Predicted) | form | Crystalline Powder | color | White to off-white | λmax | 370nm(DMF)(lit.) | CAS DataBase Reference | 2161-85-5(CAS DataBase Reference) |
| 4,6-DIACETYLRESORCINOL Usage And Synthesis |
Chemical Properties | Off-white powder | Uses | 1,1′-(4,6-Dihydroxy-1,3-phenylene)bisethanone (4,6-diacetylresorcinol, DAR) may be used in the synthesis of the following:
- Schiff base ligands
- hexadentate chalcogenated bisimine ligands
- 1,5-benzodiazepines
- ketimine of chitosan
- mannich bases
- hydrazone ligands
- thiosemicarbazone, semicarbazone and thiocarbohydrazone ligands
- binuclear cobalt(II) and copper(II) complexes
- europium (III) complexes
| Preparation | Preparation by Friedel–Crafts acylation of resorcinol, ? with acetic anhydride, – in the presence of zinc chloride at 142–150° for 15 min (96%) or at 150–160° for 20 min (68%) ; – in the presence of ferric chloride . – in the presence of concentrated sulfuric acid at 130° for 15 min (15%) ; – in the presence of 70% perchloric acid at 125–135° for 15–20 min (42%) . ? with acetyl chloride, – in the presence of zinc chloride, at 120° ; – in the presence of ferric chloride, at 150° for 15 min (60%) or at reflux for 30 min ; – in the presence of concentrated sulfuric acid (18%) . ? by a typical Friedel–Crafts reaction (24%). | General Description | 1,1′-(4,6-Dihydroxy-1,3-phenylene)bisethanone (4,6-diacetylresorcinol, DAR) is a bifunctional carbonyl compound. Its synthesis by acetylating resorcinol in the presence of zinc chloride has been reported. The crystal structure of DAR has been studied. |
| 4,6-DIACETYLRESORCINOL Preparation Products And Raw materials |
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