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4-(2-iodoethyl)phenyl 1-methylethyl ether | 1508310-71-1

中文名称
——
中文别名
——
英文名称
4-(2-iodoethyl)phenyl 1-methylethyl ether
英文别名
1-(2-Iodoethyl)-4-propan-2-yloxybenzene;1-(2-iodoethyl)-4-propan-2-yloxybenzene
4-(2-iodoethyl)phenyl 1-methylethyl ether化学式
CAS
1508310-71-1
化学式
C11H15IO
mdl
——
分子量
290.144
InChiKey
MBZXFHXZNOURLE-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

计算性质

  • 辛醇/水分配系数(LogP):
    4.2
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.45
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    4-(2-iodoethyl)phenyl 1-methylethyl ether 在 tin(II) chloride dihdyrate 、 乙醇caesium carbonate 、 Methanaminium,N-[(dimethylamino)(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)methylene]-N-methyl-, hexafluorophosphate(1-) 作用下, 以 二氯甲烷N,N-二甲基甲酰胺 为溶剂, 反应 105.17h, 生成 2-[4-(ethylsulfonyl)phenyl]-N-[1-(2-{4-[(1-methylethyl)oxy]phenyl}ethyl)-1H-indol-5-yl]acetamide
    参考文献:
    名称:
    Discovery of Tertiary Amine and Indole Derivatives as Potent RORγt Inverse Agonists
    摘要:
    A novel series of tertiary amines as retinoid-related orphan receptor gamma-t (ROR gamma t) inverse agonists was discovered through agonist/inverse agonist conversion. The level of ROR gamma t inhibition can be enhanced by modulating the conformational disruption of H12 in ROR gamma t LBD. Linker exploration and rational design led to the discovery of more potent indole-based ROR gamma t inverse agonists.
    DOI:
    10.1021/ml4003875
  • 作为产物:
    描述:
    4-羟基苯乙基溴偶氮二甲酸二异丙酯三苯基膦 、 potassium iodide 作用下, 以 四氢呋喃丙酮 为溶剂, 反应 40.0h, 生成 4-(2-iodoethyl)phenyl 1-methylethyl ether
    参考文献:
    名称:
    Discovery of Tertiary Amine and Indole Derivatives as Potent RORγt Inverse Agonists
    摘要:
    A novel series of tertiary amines as retinoid-related orphan receptor gamma-t (ROR gamma t) inverse agonists was discovered through agonist/inverse agonist conversion. The level of ROR gamma t inhibition can be enhanced by modulating the conformational disruption of H12 in ROR gamma t LBD. Linker exploration and rational design led to the discovery of more potent indole-based ROR gamma t inverse agonists.
    DOI:
    10.1021/ml4003875
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文献信息

  • Discovery of Tertiary Amine and Indole Derivatives as Potent RORγt Inverse Agonists
    作者:Ting Yang、Qian Liu、Yaobang Cheng、Wei Cai、Yingli Ma、Liuqing Yang、Qianqian Wu、Lisa A. Orband-Miller、Ling Zhou、Zhijun Xiang、Melanie Huxdorf、Wei Zhang、Jing Zhang、Jia-Ning Xiang、Stewart Leung、Yang Qiu、Zhong Zhong、John D. Elliott、Xichen Lin、Yonghui Wang
    DOI:10.1021/ml4003875
    日期:2014.1.9
    A novel series of tertiary amines as retinoid-related orphan receptor gamma-t (ROR gamma t) inverse agonists was discovered through agonist/inverse agonist conversion. The level of ROR gamma t inhibition can be enhanced by modulating the conformational disruption of H12 in ROR gamma t LBD. Linker exploration and rational design led to the discovery of more potent indole-based ROR gamma t inverse agonists.
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