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基本信息
| 产品名称 | 3-(4-氯苯基)-3-氧丙酸乙酯 |
|---|---|
| 英文名称 | Ethyl (4-chlorobenzoyl)acetate |
| 别名 | 3-氧代-3-(4-氯苯基)丙酸乙酯 |
| 英文别名 | Ethyl 3-(4-chlorophenyl)-3-oxopropanoate；Ethyl 3-Oxo-3-(4-chlorophenyl)propionate；Ethyl (4-chlorobenzoyl)acetate；3-Oxo-3-(4-chlorophenyl)propionic Acid Ethyl Ester； |
| 应用 | Ethyl (4-chlorobenzoyl)acetate may be used to synthesize 2-(carboethoxy)-3-(4′-chloro)phenylquinoxaline 1,4-dioxide. Reactant involved in: · Tandem condensation-cyclization reactions · Stereoselective ketonization-olefination of indoles · Synthesis of antiplasmodial agents · SIRT 1/2 inhibitor preparation for use as antitumor agents · Synthesis of mineralocorticoid receptor antagonists · Intramolecular Michael addition reactions |
| 规格或纯度 | 98% |
| 运输条件 | 冰袋运输 |
一般描述
Ethyl (4-chlorobenzoyl)acetate may be used to synthesize 2-(carboethoxy)-3-(4′-chloro)phenylquinoxaline 1,4-dioxide. Reactant involved in: · Tandem condensation-cyclization reactions · Stereoselective ketonization-olefination of indoles · Synthesis of antiplasmodial agents · SIRT 1/2 inhibitor preparation for use as antitumor agents · Synthesis of mineralocorticoid receptor antagonists · Intramolecular Michael addition reactions
Ethyl (4-chlorobenzoyl)acetate may be used to synthesize 2-(carboethoxy)-3-(4′-chloro)phenylquinoxaline 1,4-dioxide. Reactant involved in: · Tandem condensation-cyclization reactions · Stereoselective ketonization-olefination of indoles · Synthesis of antiplasmodial agents · SIRT 1/2 inhibitor preparation for use as antitumor agents · Synthesis of mineralocorticoid receptor antagonists · Intramolecular Michael addition reactions
安全信息
| 闪点（摄氏） | 128 °C |
|---|
相关属性
| CAS编号 | 2881-63-2 |
|---|---|
| 折光率 | 1.55 |
| 熔点 | 34 °C |
| 沸点 | 268-269 °C |
| 溶解性 | 可溶于丙酮 |
| 储存温度 | 2-8°C储存 |
| MDL号 | MFCD00018713 |
| 密度 | 1.218 |
| 分子量 | 226.66 |
| 分子式 | ClC6H4COCH2CO2C2H5 |
| 品牌 | 阿拉丁 |
| PubChem CID | 101336 |