暂无可渲染的结构数据
COC(=O)C(=O)C(C1=CC=CC=C1F)Cl中间体产品
methyl 3-chloro-3-(2-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-(2-氟苯基)-2-氧代丙酸乙酯 |
|---|---|
| English name | methyl 3-chloro-3-(2-fluorophenyl)-2-oxopropanoate |
| IUPAC 名称 | — |
| CAS号 | 1007875-06-0 |
| 数据库编号 | 54289762 |
| 分子式 | — |
| 分子量 | — |
产品信息
甲基 3-氯-3-(2-氟苯基)-2-氧代丙酸乙酯（CAS 1007875-06-0）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 54289762
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
11 条反应 · 11 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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.89 min; [M+H]+=252.0.
来源 ID: ord-6ac341c522ec42e5b7fb6d8d8046640f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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.76 min; [M+H]+=253.2.
来源 ID: ord-ec7011243a55449d9f8b0906743d2640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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.76 min; [M+H]+=253.2.
来源 ID: ord-ec7011243a55449d9f8b0906743d2640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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.89 min; [M+H]+=252.0.
来源 ID: ord-948cff0ff0164719a0cd052c970d3605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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.89 min; [M+H]+=252.0.
来源 ID: ord-948cff0ff0164719a0cd052c970d3605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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.76 min; [M+H]+=253.2.
来源 ID: ord-b74a58989fea465ab98f6e8dafded3bb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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with cyclopropanecarbothioic acid amide. LC-MS: tR=1.00 min; [M+H]+=278.3.
来源 ID: ord-afb000d7a35e4291861a7c1a0be0b36d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: This compound was synthesised as 3-chloro-3-(4-fluoro-phenyl)-2-oxo-propionic acid methyl ester but using 2-fluorobenzaldehyde instead 4-fluorobenzaldehyde.
来源 ID: ord-51814fc563a14ecf9a85d57309251d67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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.89 min; [M+H]+=252.0.
来源 ID: ord-6ac341c522ec42e5b7fb6d8d8046640f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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thiourea. LC-MS: tR=0.76 min; [M+H]+=253.2.
来源 ID: ord-ec7011243a55449d9f8b0906743d2640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-(2-fluoro-phenyl)-2-oxo-propionic acid methyl ester with thioacetamide. LC-MS: tR=0.89 min; [M+H]+=252.0.
来源 ID: ord-948cff0ff0164719a0cd052c970d3605PubChem 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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