产品描述
| 沸点 | 237°C |
| 折光率 | 1.45 |
| 敏感性 | 对热敏感 |
| 溶解性 | Insoluble in water. |
| 存贮条件 | 储存温度2-8℃ |
| 密度 | 1.1880 |
| 应用 |
4-Vinyl-1,3-dioxolan-2-one may be used in the preparation of 2-arylbenzo[d]thiazole scaffolds. It may be used in the synthesis of the following multi-functional cyclic carbonates: . 4,4′-((hexane-1,6-diylbis(sulfanediyl))bis-(ethane-2,1-diyl))bis(1,3-dioxolan-2-one) (Bis-CC) . 2-ethyl-2-(((3-((2-(2-oxo-1,3-dioxolan-4-yl)-ethyl)thio)propanoyl)oxy) methyl)propane-1,3-diyl bis(3-((2-(2-oxo-1,3-dioxolan-4-yl)ethyl)thio)propanoate) (Tris-CC) . 2,2-bis(((3-((2-(2-oxo-1,3-dioxolan-4-yl)ethyl)-thio)propanoyl)oxy) methyl)propane-1,3-diyl bis(3-((2-(2-oxo-1,3-dioxolan-4-yl)ethyl)thio)propanoate) (Tetra-CC) Used to synthesize functional polymers. |
| 产品介绍 | 4-Vinyl-1,3-dioxolan-2-one (VEC) is a cyclic carbonate, that can be synthesized from acrolein by reacting with sulfur ylide and CO2. The ruthenium-catalyzed transfer hydrogenation (TH) of VEC in the presence of 2-propanol forms 1,2-butanediol. Indolines and indoles undergo selective C-H allylation with VEC in the presence of rhodium(III) catalyst. |
| 别名 | 4-乙烯基-1,3-二氧戊环-2-酮; 乙烯基碳酸亚乙酯; VEC;Vinyl ethylene carbonate; 2-Oxo-4-vinyl-1,3-dioxolane; VEC |
