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| Product | Description | |
|---|---|---|
| Diallyl carbonate | Diallyl carbonate is an acrylating agent. Allyl carbonates are widely employed in Tsuji-Trost allylation, generating carbanion, boronate, phosphide, amide and alkoxide, nucleophiles in situ and improving reaction rates over allyl acetate. Allyl carbonates are also of considerable interest for the intramolecular decarboxylative assymetric couplings. Uses: Transesterification of diallyl carbonate with glycerol in the presence of a catalyst (pd/pph3), generates glycerol carbonate. Group: Polymer/macromoleculeallyl monomers. Alternative Names: Allyl carbonate; Carbonic acid, di-2-propenyl ester. CAS No. 15022-08-9. Molecular formula: C7H10O3. Mole weight: 142.15 g/mol. Purity: 0.95. Canonical SMILES: C=CCOC(=O)OCC=C. Density: 0.991 g/mL at 25 °C (lit.). ECNumber: 239-106-9. Catalog: ACM-MO-15022089. |  |
| DIALLYL CARBONATE | Transesterification of diallyl carbonate with glycerol in the presence of a catalyst (Pd/PPh3), generates glycerol carbonate. Synonyms: Allyl carbonate; Carbonic acid, di-2-propenyl ester; Carbonic acid, diallyl ester; carbonicacid,di-2-propenylester; DIALLYL CARBONATE; Carbonic acid diallyl. Grades: 95%. CAS No. 15022-08-9. Molecular formula: C7H10O3. Mole weight: 142.15. |  |
| Diallyl pyrocarbonate | Allyloxycarbonylation (Alloc) Reagents. Alternative Names: (Alloc)2O, Diallyl dicarbonate. CAS No. 115491-93-5. Molecular formula: C8H10O5. Mole weight: 186.16. Purity: 0.95. IUPACName: prop-2-enoxycarbonyl prop-2-enyl carbonate. Density: 1.121 g/mL at 25ºC(lit.). Catalog: ACM115491935. | |
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