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4-(2-Hexyl-oxazol-5-yl)-benzenesulfonyl chloride | 293306-74-8

中文名称
——
中文别名
——
英文名称
4-(2-Hexyl-oxazol-5-yl)-benzenesulfonyl chloride
英文别名
4-(2-Hexyl-1,3-oxazol-5-yl)benzenesulfonyl chloride;4-(2-hexyl-1,3-oxazol-5-yl)benzenesulfonyl chloride
4-(2-Hexyl-oxazol-5-yl)-benzenesulfonyl chloride化学式
CAS
293306-74-8
化学式
C15H18ClNO3S
mdl
——
分子量
327.832
InChiKey
YROOKQGHDTVEMW-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):
    4.8
  • 重原子数:
    21
  • 可旋转键数:
    7
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    68.6
  • 氢给体数:
    0
  • 氢受体数:
    4

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-Hexyl-oxazol-5-yl)-benzenesulfonyl chloride吡啶盐酸 作用下, 以 甲醇二氯甲烷 为溶剂, 生成 4-(2-Hexyl-oxazol-5-yl)-N-{4-[2-((R)-2-hydroxy-2-pyridin-3-yl-ethylamino)-ethyl]-phenyl}-benzenesulfonamide
    参考文献:
    名称:
    Substituted oxazole benzenesulfonamides as potent human β3 adrenergic receptor agonists
    摘要:
    As a part of our investigation into the development of orally bioavailable beta(3) adrenergic receptor agonists, we have identified a series of substituted oxazole derivatives that are potent beta(3) agonists with excellent selectivity against other beta receptors. Several of these compounds showed excellent oral bioavailability in dogs. One example, cyclopentylethyloxazole 5f is a potent beta(3) agonist (EC50 = 14 nM, 84% activation) with 340-fold and 160-fold selectivity over beta(1) and beta(2) receptors, respectively, and has 38% oral bioavailability in dogs. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00277-8
  • 作为产物:
    参考文献:
    名称:
    Substituted oxazole benzenesulfonamides as potent human β3 adrenergic receptor agonists
    摘要:
    As a part of our investigation into the development of orally bioavailable beta(3) adrenergic receptor agonists, we have identified a series of substituted oxazole derivatives that are potent beta(3) agonists with excellent selectivity against other beta receptors. Several of these compounds showed excellent oral bioavailability in dogs. One example, cyclopentylethyloxazole 5f is a potent beta(3) agonist (EC50 = 14 nM, 84% activation) with 340-fold and 160-fold selectivity over beta(1) and beta(2) receptors, respectively, and has 38% oral bioavailability in dogs. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00277-8
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