反应 #3880015
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-29641de841c8479296793615146a7116暂无可渲染的结构数据
C1CCC(CC1)CCl产品信息
氯甲基环己烷(CAS 26895-68-1)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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9 条反应 · 9 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-29641de841c8479296793615146a7116反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-ea1f4b32a10944538c3eada0515232b9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The preparation is carried out as in Example 36 with cyclohexylmethyl chloride and sodium [1-(triphenylmethyl)imidazol-4-yl]methoxide. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether
来源 ID: ord-fed2e066e3b445f18822c21fcc95eac4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The preparation is carried out as in Example 36 with cyclohexylmethyl chloride and sodium [1-(triphenylmethyl)imidazol-4-yl]methoxide. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether
来源 ID: ord-adca1c80bf37432094417255893383ad反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: (melting point: 104° C.) was prepared by the method described in 1.1 by substituting, on an equimolar basis, 4-hydroxy-cinnamic acid methyl ester and chloromethyl cyclohexane for the 4-hydroxybenzoic acid methyl ester and 4-(1,1,3-trimethyl-2-cyclohexyl)-2-butyl chloride used in Example 1.1. (melting point: 104° C.) was prepared by the method
来源 ID: ord-f9541eacbb4348afbe800a311fa17c53反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Using 5,6-bis(4-methoxyphenyl)-4-cyano-2H-pyridazin-3-one and cyclohexylmethyl chloride as starting materials, the procedures of Example 1 were repeated likewise, whereby the title compound was obtained in a yield of 45.0%.
来源 ID: ord-95353cb5f6e345f591e97dc3b54b745d反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The preparation is carried out as in Example 36 with cyclohexylmethyl chloride and sodium [1-(triphenylmethyl)imidazol-4-yl]methoxide. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether
来源 ID: ord-f0fc52df68f643bab1bef0ece779178a反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The preparation is carried out as in Example 36 with cyclohexylmethyl chloride and sodium [1-(triphenylmethyl)imidazol-4-yl]methoxide. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether
来源 ID: ord-fed2e066e3b445f18822c21fcc95eac4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The preparation is carried out as in Example 36 with cyclohexylmethyl chloride and sodium [1-(triphenylmethyl)imidazol-4-yl]methoxide. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether. The title compound is crystallized in the hydrogenmaleate form from ethanol/diethyl ether
来源 ID: ord-adca1c80bf37432094417255893383adPubChem References
以下资料来自该化合物的公开数据库参考记录。
