暂无可渲染的结构数据
COC(=O)C(=O)C(C1=CC(=CC=C1)F)Cl中间体产品
methyl 3-chloro-3-(3-fluorophenyl)-2-oxopropanoate
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | 甲基 3-氯-3-(3-氟苯基)-2-氧代丙酸乙酯 |
|---|---|
| English name | methyl 3-chloro-3-(3-fluorophenyl)-2-oxopropanoate |
| IUPAC 名称 | — |
| CAS号 | 1007874-03-4 |
| 数据库编号 | 57437155 |
| 分子式 | — |
| 分子量 | — |
产品信息
甲基 3-氯-3-(3-氟苯基)-2-氧代丙酸乙酯（CAS 1007874-03-4）的产品身份、结构标识及相关反应资料，供化学中间体检索、研发和采购评估使用。
可能的应用方向
仅供专业研发与工业用途
数据库编号 57437155
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.78 min; [M+H]+=252.9.
来源 ID: ord-b1848f6b81fd40a7803b271a877b2e04反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.91 min; [M+H]+=252.1.
来源 ID: ord-ba582309925646ac867f937e7ca74d9b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.91 min; [M+H]+=252.1.
来源 ID: ord-f522974fe72a4223b3675864d02e2384反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.91 min; [M+H]+=252.1.
来源 ID: ord-f522974fe72a4223b3675864d02e2384反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.78 min; [M+H]+=252.9.
来源 ID: ord-b9726f3b8a294c6d97c510768221a605反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with cyclopropanecarbothioic acid amide.
来源 ID: ord-4f04746d807d4fec974d64fecc992f78反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.91 min; [M+H]+=252.1.
来源 ID: ord-f745194238c340c89e3f90b5552df975反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.78 min; [M+H]+=252.9.
来源 ID: ord-b1848f6b81fd40a7803b271a877b2e04反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.78 min; [M+H]+=252.9.
来源 ID: ord-b1848f6b81fd40a7803b271a877b2e04反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.91 min; [M+H]+=252.1.
来源 ID: ord-ba582309925646ac867f937e7ca74d9b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.91 min; [M+H]+=252.1.
来源 ID: ord-ba582309925646ac867f937e7ca74d9b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: prepared by reaction of 3-chloro-3-(3-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.78 min; [M+H]+=252.9.
来源 ID: ord-08cf186e322b4d6aa5c361cbb69cc2bbPubChem References
以下资料来自该化合物的公开数据库参考记录。
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