反应 #4053939
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ee970e8daadd4f8b922b4b517e8cbe3c暂无可渲染的结构数据
C1=CC(=C(C=C1C(=O)N)Cl)F产品信息
3-氯-4-氟苯甲酰胺(CAS 701-43-9)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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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ee970e8daadd4f8b922b4b517e8cbe3c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c9f1c4ee51c84a94be9a409530ad7933反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ff2b3c008abc4255b062330fca7f4e8a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fe5883cc23304df0a59eba6e1decbb63反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ee970e8daadd4f8b922b4b517e8cbe3c反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-c9f1c4ee51c84a94be9a409530ad7933反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ff2b3c008abc4255b062330fca7f4e8a反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fe5883cc23304df0a59eba6e1decbb63反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The same method as in Example 1 was conducted using 5-ethyl-4,5,6,7-tetrahydrofuro[3,2-c]pyridin-7-ol (Reference Example 34) instead of 6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-4-ol (Reference Example 6) and was conducted using 4-carbamoyl-2-chloro-1-fluorobenzene instead of 1-fluoronaphthalene to give the objective compound. to give the objective compound
来源 ID: ord-b60bcd60cb2c4931b1e305a2f37b0d59反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The same method as in Example 1 was conducted using 4,5,6,7-tetrahydrofuro[3,2-c]pyridin-7-ol (Reference Example 33) instead of 6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-4-ol (Reference Example 6) and was conducted using 4-carbamoyl-2-chloro-1-fluorobenzene instead of 1-fluoronaphthalene to give the objective compound. to give the objective compound
来源 ID: ord-fb9e39f311d04075bf491bf4d875b21e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The same method as in Example 1 was conducted using 6-ethyl-5,6,7,8-tetrahydro-4H-thieno[2,3-d]azepin-4-ol (Reference Example 45) instead of 6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-4-ol (Reference Example 6) and was conducted using 4-carbamoyl-2-chloro-1-fluorobenzene instead of 1-fluoronaphthalene to give the objective compound. to give the objective compound
来源 ID: ord-bea77065f57841e3af636dc74c707ed7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The same method as in Example 3 was conducted using 6-methyl-5,6,7,8-tetrahydro-4H-thieno[2,3-d]azepin-4-ol (Reference Example 28) instead of 6-methyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridin-4-ol (Reference Example 6) and was conducted using 4-carbamoyl-2-chloro-1-fluorobenzene instead of 1,3-difluorobenzene to give the objective compound. to give the objective compound
来源 ID: ord-657f616a323f499fa01b7653a9315615PubChem References
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