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89-84-9 2’,4’-Dihydroxyacetophenone
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* For R&D use only.In Production Stage,Request Bulk Quotation
| Brand | CatalogID | Unit | Price($) | Stock (US) | Stock (CN) | Ships within | Quantity | Buy | |||||||||||
| Accela | SY004020 | 5g | 10.00 | 0 | in stock | 3-5 days | Login | ||||||||||||
| Accela | SY004020 | 10g | 10.00 | 0 | in stock | 3-5 days | Login | ||||||||||||
| Accela | SY004020 | 25g | 10.00 | 0 | in stock | 3-5 days | Login | ||||||||||||
| Accela | SY004020 | 100g | 30.00 | in stock | 0 | 1 day | Login | ||||||||||||
| Accela | SY004020 | 500g | 96.00 | 0 | 0 | inquire | Login | ||||||||||||
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Product InformationSafety InformationReferences
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The position of O-alkylation can be varied by suitable choice of reagent. Thus, NaH in DMSO followed by MeI gives predominantly the 2-alkylated product, whereas Li2CO3 in DMF favors 4-alkylation. The latter is a fairly general method for the alkylation of phenols, thiophenols and ?-diketones with pKa less than about 8: Synth. Commun., 18, 1379 (1988).
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