反应 #4126178
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-93fe1968d41447758b90a99bdc7cad0e暂无可渲染的结构数据
C1=CC(=CC=C1C(=O)CCCCCl)Cl产品信息
5-氯-1-(4-氯苯基)戊-1-one(CAS 945-97-1)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-93fe1968d41447758b90a99bdc7cad0e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b3ebe1ff4c234b0ab541ece3bbe14108反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-93fe1968d41447758b90a99bdc7cad0e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-b3ebe1ff4c234b0ab541ece3bbe14108反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme E using 5-chloro-1-(4-chlorophenyl)-1-pentanone and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 441.1 (M+H)+. Prepared by Procedure K and Scheme E
来源 ID: ord-b5dfbc1b699048f2aa7124fbd15d7932反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme B1 (K2CO3) using 1-(4-chlorophenyl)-5-chloro-1-pentanone and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 441.1 (M+H)+.
来源 ID: ord-f016710ef12a45f1b240ae0d5b5ebe48反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme B1 using 5-chloro-1-(4-chlorophenyl)-1-pentanone and N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 427.1 (M+H)+. Prepared by Procedure K and Scheme B1
来源 ID: ord-de35025ec5114fa99de1ebb488a60570反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme B1 using 5-chloro-1-(4-chlorophenyl)-1-pentanone and N-[3-(4-piperidinyl)phenyl]cyclopropanecarboxamide: ESMS m/e: 439.1 (M+H)+. Prepared by Procedure K and Scheme B1
来源 ID: ord-88de191808504a67bb66922184edcdfa反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme E using 5-chloro-1-(4-chlorophenyl)-1-pentanone and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 441.1 (M+H)+. Prepared by Procedure K and Scheme E
来源 ID: ord-ff3f09afaffd4410ba2b323faae49365反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme B1 (K2CO3) using 1-(4-chlorophenyl)-5-chloro-1-pentanone and 2-methyl-N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 441.1 (M+H)+.
来源 ID: ord-58a1e973caed406aae472f4bdc5436ae反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme B1 using 5-chloro-1-(4-chlorophenyl)-1-pentanone and N-[3-(4-piperidinyl)phenyl]propanamide: ESMS m/e: 427.1 (M+H)+. Prepared by Procedure K and Scheme B1
来源 ID: ord-8b4c8c5a98074d6cb5c36dc647fe315c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Prepared by Procedure K and Scheme B1 using 5-chloro-1-(4-chlorophenyl)-1-pentanone and N-[3-(4-piperidinyl)phenyl]cyclopropanecarboxamide: ESMS m/e: 439.1 (M+H)+. Prepared by Procedure K and Scheme B1
来源 ID: ord-3dd16df380384c1d8472e3051159964dPubChem 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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