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(R)-6-(4-(dimethylamino)phenyl)-4-(naphthalen-2-yl)cyclohexa-1,3-dienecarbaldehyde | 1071780-60-3

中文名称
——
中文别名
——
英文名称
(R)-6-(4-(dimethylamino)phenyl)-4-(naphthalen-2-yl)cyclohexa-1,3-dienecarbaldehyde
英文别名
——
(R)-6-(4-(dimethylamino)phenyl)-4-(naphthalen-2-yl)cyclohexa-1,3-dienecarbaldehyde化学式
CAS
1071780-60-3
化学式
C25H23NO
mdl
——
分子量
353.464
InChiKey
ALAKFUJGJWSMIJ-VWLOTQADSA-N
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

反应信息

  • 作为产物:
    描述:
    (R)-2-isopropyl-5-methylcyclohexyl 2-((6-(4-(dimethylamino)phenyl)-4-(naphthalen-2-yl)cyclohexa-1,3-dienyl)methylene)hydrazinecarboxylate 在 硫酸 作用下, 以 乙醇 为溶剂, 反应 2.5h, 生成 (R)-6-(4-(dimethylamino)phenyl)-4-(naphthalen-2-yl)cyclohexa-1,3-dienecarbaldehyde
    参考文献:
    名称:
    Synthesis and cellular effects of cycloterpenals: Cyclohexadienal-based activators of neurite outgrowth
    摘要:
    An unusual class of diterpenoid natural products, 'cycloterpenals' ( with a central cyclohexadienal core), that arise in nature by condensation of retinoids and other isoprenes, have been isolated from a variety of organisms including marine sponges as well as from the human eye. A milk whey protein has also demonstrated the formation of a cycloterpenal derived from beta-ionylidineacetaldehyde. Here, we generate a synthetic library of these molecules where we detail reaction conditions required to effect cross condensation of alpha,beta-unsaturated aldehydes as opposed to homodimerization. The ability of this class of molecules to activate neurite outgrowth activity is reported. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2008.07.030
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