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反式苯基肉桂砜（CAS 16212-06-9）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。
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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: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaidehyde (0.01 mol) was subjected to the Procedure 1. The title compound was obtained in 68-72% yield.
来源 ID: ord-ba82acd4778145d2b83d56e56ab397bf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaidehyde (0.01 mol) was subjected to the Procedure 1. The title compound was obtained in 68-72% yield.
来源 ID: ord-ba82acd4778145d2b83d56e56ab397bf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1, Part B. The title compound was obtained in 68-72% yield.
来源 ID: ord-1d2ba8c688264de28bc4e4a9d5ccbfaa反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1, Part B. The title compound was obtained in 68-72% yield.
来源 ID: ord-1d2ba8c688264de28bc4e4a9d5ccbfaa反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1, Part B. The title compound was obtained in 68-72% yield.
来源 ID: ord-4ad4e79f7fdb4a308ab46c99524ae40f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaidehyde (0.01 mol) was subjected to the Procedure 1. The title compound was obtained in 68-72% yield.
来源 ID: ord-ba82acd4778145d2b83d56e56ab397bf反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1, Part B. The title compound was obtained in 68-72% yield.
来源 ID: ord-b703a47f99884a0ab6e87ea5fd2fcbe6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1. The title compound was obtained in 68-72% yield.
来源 ID: ord-83ec8352a0a0489ab4cef0d2f12d099b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1, Part B. The title compound was obtained in 68-72% yield.
来源 ID: ord-1d2ba8c688264de28bc4e4a9d5ccbfaa反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaldehyde (0.01 mol) was subjected to the Procedure 1, Part B. The title compound was obtained in 68-72% yield.
来源 ID: ord-4ad4e79f7fdb4a308ab46c99524ae40f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of phenyl sulfonylacetic acid (0.01 mol) and benzaidehyde (0.01 mol) was subjected to the Procedure 1. The title compound was obtained in 68-72% yield.
来源 ID: ord-ba82acd4778145d2b83d56e56ab397bfPubChem References
以下资料来自该化合物的公开数据库参考记录。