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3-iodo-4-(6-methoxynaphthalen-2-yl)butan-2-one | 1225055-59-3

中文名称
——
中文别名
——
英文名称
3-iodo-4-(6-methoxynaphthalen-2-yl)butan-2-one
英文别名
3-Iodo-4-(6-methoxynaphthalen-2-yl)butan-2-one
3-iodo-4-(6-methoxynaphthalen-2-yl)butan-2-one化学式
CAS
1225055-59-3
化学式
C15H15IO2
mdl
——
分子量
354.187
InChiKey
IDHUYOUBCMRXRZ-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):
    3.9
  • 重原子数:
    18
  • 可旋转键数:
    4
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

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

  • 作为产物:
    描述:
    萘丁美酮N-碘代丁二酰亚胺三氟甲磺酸 作用下, 以 乙腈 为溶剂, 以75%的产率得到4-(5-iodo-6-methoxynaphthalen-2-yl)butan-2-one
    参考文献:
    名称:
    Mild Arming and Derivatization of Natural Products via an In(OTf)3-Catalyzed Arene Iodination
    摘要:
    Iodination of arene-containing natural products employing N-iodosuccinimide catalyzed by In(OTf)(3) at ambient temperature is reported as a versatile and mild method for natural product derivatization amenable to small scale. This process facilitates natural product derivatization of arene moieties for SAR studies, homo- and heterodimerization of natural products, and also conjugation with reporters such as biotin via subsequent metal-mediated coupling reactions.
    DOI:
    10.1021/ol100587j
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文献信息

  • Mild Arming and Derivatization of Natural Products via an In(OTf)<sub>3</sub>-Catalyzed Arene Iodination
    作者:Cong-Ying Zhou、Jing Li、Satyamaheshwar Peddibhotla、Daniel Romo
    DOI:10.1021/ol100587j
    日期:2010.5.7
    Iodination of arene-containing natural products employing N-iodosuccinimide catalyzed by In(OTf)(3) at ambient temperature is reported as a versatile and mild method for natural product derivatization amenable to small scale. This process facilitates natural product derivatization of arene moieties for SAR studies, homo- and heterodimerization of natural products, and also conjugation with reporters such as biotin via subsequent metal-mediated coupling reactions.
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