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2,2,13,13-tetramethyl-tetradecane-3,12-dione | 54622-11-6

中文名称
——
中文别名
——
英文名称
2,2,13,13-tetramethyl-tetradecane-3,12-dione
英文别名
2,2,13,13-Tetramethyltetradecane-3,12-dione
2,2,13,13-tetramethyl-tetradecane-3,12-dione化学式
CAS
54622-11-6
化学式
C18H34O2
mdl
——
分子量
282.467
InChiKey
ZZNBRQZJWMUXBR-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):
    5.2
  • 重原子数:
    20
  • 可旋转键数:
    11
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.89
  • 拓扑面积:
    34.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Layered Compounds. XVIII. Synthesis of a Paracyclophane Containing the 1,2,3,4,5-Hexapentaene Group and the Stereochemistry of Its Formation
    摘要:
    为了研究跨annular 电子相互作用,我们从环状二炔二醇 IX 通过二烯二溴化物 X 合成了新型环状 1,2,3,4,5-hexapentaene 化合物。从二炔二醇异构体 IXc-I 中得到的二炔二溴化物 Xc-I 与活性锌脱溴后得到环己五烯 IIc,而从第二个二炔二醇异构体 IXc-II 中得到的另一种二炔二溴化物 Xc-II 则没有脱溴。随后对二溴化物 Xc-I 进行了 X 射线晶体学分析,并确定了该二溴化物的 s-trans 结构。在这一结果的基础上,讨论了从二炔二醇转变到六方戊烯基团的立体化学过程。含有己五烯基团的环烷 IIa 的电子能谱显示,苯环与己五烯基团之间存在反π电子相互作用,这与其他己五烯衍生物 IIc 和 XV 不同。
    DOI:
    10.1246/bcsj.47.2398
  • 作为产物:
    参考文献:
    名称:
    Petrov,A.D. et al., Journal of general chemistry of the USSR, 1960, vol. 30, p. 1124 - 1133
    摘要:
    DOI:
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文献信息

  • Drugs With Improved Hydrophobicity For Incorporation in Medical Devices
    申请人:Desai Neil P.
    公开号:US20090130163A1
    公开(公告)日:2009-05-21
    The invention provides a medical device comprising a hydrophobic analog of a medicament known to inhibit cell proliferation and migration. The invention also provides a method of treating a narrowing in a body passageway comprising placing an implantable medical device comprising a hydrophobic analog of a medicament known to inhibit cell proliferation and migration. The medicaments can be incorporated within or coated on the device. The invention further provides hydrophobic analogs of medicaments known to inhibit cell proliferation and migration.
    本发明提供了一种医疗设备,包括一种疏性类似于已知抑制细胞增殖和迁移的药物的药物。本发明还提供了一种治疗体内狭窄通道的方法,包括放置一种可植入的医疗设备,其中包括一种疏性类似于已知抑制细胞增殖和迁移的药物。药物可以被纳入或涂覆在设备上。本发明还提供了疏性类似于已知抑制细胞增殖和迁移的药物。
  • NANOPARTICLE FORMULATIONS AND USES THEREOF
    申请人:Desai Neil P.
    公开号:US20090263483A1
    公开(公告)日:2009-10-22
    The present invention provides compositions comprising nanoparticles comprising: 1) a drug, such as a hydrophobic drug derivative; and 2) a carrier protein. Also provided are methods of treating diseases (such as cancer) using the compositions, as well as kits and unit dosages.
    本发明提供了包含纳米颗粒的组合物,包括:1)药物,如疏性药物衍生物;和2)载体蛋白质。还提供了使用该组合物治疗疾病(如癌症)的方法,以及套件和单元剂量。
  • NANOPARTICLE FORMULATIONS AND USES THEROF
    申请人:Abraxis BioScience, LLC
    公开号:US20140302157A1
    公开(公告)日:2014-10-09
    The present invention provides compositions comprising nanoparticles comprising: 1) a drug, such as a hydrophobic drug derivative; and 2) a carrier protein. Also provided are methods of treating diseases (such as cancer) using the compositions, as well as kits and unit dosages.
    本发明提供了包含纳米颗粒的组合物,其中纳米颗粒包括:1)药物,如疏性药物衍生物;和2)载体蛋白。还提供了使用该组合物治疗疾病(如癌症)的方法,以及配套工具和单元剂量。
  • DRUGS WITH IMPROVED HYDROPHOBICITY FOR INCORPORATION IN MEDICAL DEVICES
    申请人:Abraxis BioScience, LLC
    公开号:US20150190556A1
    公开(公告)日:2015-07-09
    The invention provides a medical device comprising a hydrophobic analog of a medicament known to inhibit cell proliferation and migration. The invention also provides a method of treating a narrowing in a body passageway comprising placing an implantable medical device comprising a hydrophobic analog of a medicament known to inhibit cell proliferation and migration. The medicaments can be incorporated within or coated on the device. The invention further provides hydrophobic analogs of medicaments known to inhibit cell proliferation and migration.
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