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Phenyl 8-bromo-2-[(2-methylpropan-2-yl)oxycarbonyloxy]naphthalene-1-carboxylate

中文名称
——
中文别名
——
英文名称
Phenyl 8-bromo-2-[(2-methylpropan-2-yl)oxycarbonyloxy]naphthalene-1-carboxylate
英文别名
phenyl 8-bromo-2-[(2-methylpropan-2-yl)oxycarbonyloxy]naphthalene-1-carboxylate
Phenyl 8-bromo-2-[(2-methylpropan-2-yl)oxycarbonyloxy]naphthalene-1-carboxylate化学式
CAS
——
化学式
C22H19BrO5
mdl
——
分子量
443.3
InChiKey
LHFDSBSPGYQOKP-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):
    6.4
  • 重原子数:
    28
  • 可旋转键数:
    7
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    61.8
  • 氢给体数:
    0
  • 氢受体数:
    5

文献信息

  • SYNTHESIS OF TETRACYCLINES AND ANALOGUES THEREOF
    申请人:President and Fellows of Harvard College
    公开号:US20140163238A1
    公开(公告)日:2014-06-12
    The tetracycline class of antibiotics has played a major role in the treatment of infectious diseases for the past 50 years. However, the increased use of the tetracyclines in human and veterinary medicine has led to resistance among many organisms previously susceptible to tetracycline antibiotics. The modular synthesis of tetracyclines and tetracycline analogs described provides an efficient and enantioselective route to a variety of tetracycline analogs and polycyclines previously inaccessible via earlier tetracycline syntheses and semi-synthetic methods. These analogs may be used as anti-microbial agents or anti-proliferative agents in the treatment of diseases of humans or other animals.
  • US9365493B2
    申请人:——
    公开号:US9365493B2
    公开(公告)日:2016-06-14
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