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6-tert-butylchroman-8-carbaldehyde | 1165739-46-7

中文名称
——
中文别名
——
英文名称
6-tert-butylchroman-8-carbaldehyde
英文别名
——
6-tert-butylchroman-8-carbaldehyde化学式
CAS
1165739-46-7
化学式
C14H18O2
mdl
——
分子量
218.296
InChiKey
DVGUBYIWGWLFCY-UHFFFAOYSA-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

  • 作为反应物:
    描述:
    丙二酸6-tert-butylchroman-8-carbaldehyde哌啶吡啶 作用下, 反应 2.0h, 以86%的产率得到(E)-3-(6-tert-butylchroman-8-yl)acrylic acid
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of novel diarylalkyl amides as TRPV1 antagonists
    摘要:
    We have developed a new class of diarylalkyl amides as novel TRPV1 antagonists. They exhibited potent Ca-45(2+) uptake inhibitions in rat DRG neuron. In particular, the amide 59 was identified as a potent antagonist with IC50 of 57 nM. The synthesis and structure-activity relationship of the diarylalkyl amides are also described. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.04.010
  • 作为产物:
    描述:
    N,N-二甲基甲酰胺叔丁基锂 作用下, 以 四氢呋喃正己烷 为溶剂, 反应 0.5h, 生成 6-tert-butylchroman-8-carbaldehyde
    参考文献:
    名称:
    Design, synthesis, and biological evaluation of novel diarylalkyl amides as TRPV1 antagonists
    摘要:
    We have developed a new class of diarylalkyl amides as novel TRPV1 antagonists. They exhibited potent Ca-45(2+) uptake inhibitions in rat DRG neuron. In particular, the amide 59 was identified as a potent antagonist with IC50 of 57 nM. The synthesis and structure-activity relationship of the diarylalkyl amides are also described. (C) 2009 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmc.2009.04.010
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