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766-39-2 2,3-Dimethylmaleic Anhydride
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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 | SY008056 | 5g | 10.00 | 0 | in stock | 3-5 days | Login | ||||||||||||
| Accela | SY008056 | 10g | 10.00 | 0 | in stock | 3-5 days | Login | ||||||||||||
| Accela | SY008056 | 25g | 10.00 | in stock | in stock | 1 day | Login | ||||||||||||
| Accela | SY008056 | 100g | 30.00 | in stock | in stock | 1 day | Login | ||||||||||||
| Accela | SY008056 | 500g | 90.00 | 0 | in stock | 3-5 days | Login | ||||||||||||
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Product InformationSafety InformationReferences
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Does not undergo Diels-Alder reactions with furan, but does react with 1,3-Diphenyl-isobenzofuran, to give benzocantharadin: J. Org. Chem., 47, 4011 (1982). The use of the dimethylmaleoyl (DMM) group has been investigated for amino group protection in oligosaccharide synthesis. The DMM group is introduced using triethylamine as base. It promotes ? -linkage by neighboring group participation and is stable to acids and non-nucleophilic bases. Cleavage can be brought about by treatment with dilute aqueous NaOH: Eur. J. Org. Chem., 2305 (1998).
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