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[(8R,9S,13S,14S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] bicyclo[2.2.1]hept-5-ene-2-carboxylate | 1119900-16-1

中文名称
——
中文别名
——
英文名称
[(8R,9S,13S,14S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] bicyclo[2.2.1]hept-5-ene-2-carboxylate
英文别名
——
[(8R,9S,13S,14S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] bicyclo[2.2.1]hept-5-ene-2-carboxylate化学式
CAS
1119900-16-1
化学式
C26H30O3
mdl
——
分子量
390.522
InChiKey
JJXQDUGXSPBJQV-AJVHZSFNSA-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

物化性质

  • 沸点:
    539.6±50.0 °C(predicted)
  • 密度:
    1.198±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.6
  • 重原子数:
    29
  • 可旋转键数:
    3
  • 环数:
    6.0
  • sp3杂化的碳原子比例:
    0.62
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 氢受体数:
    3

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:
    雌酚酮5-norbornene-endo-2-carbonyl chloride吡啶 作用下, 反应 0.5h, 以60%的产率得到[(8R,9S,13S,14S)-13-methyl-17-oxo-7,8,9,11,12,14,15,16-octahydro-6H-cyclopenta[a]phenanthren-3-yl] bicyclo[2.2.1]hept-5-ene-2-carboxylate
    参考文献:
    名称:
    Ring-opening metathesis polymerization of steroid-conjugated norbornenes and gradual release of estrone from a polymer film
    摘要:
    Steroids (estrone, estradiol, ursodeoxycholic acid, chenodeoxycholic acid, cortisone, prednisone, and dexamethasone) were reacted with either 5-norbornene-2-carboxylic acid chloride or 5-norbornene-2-methanol to form new norbornene derivatives with bioactive and sterically demanding steroid residues bound with an ester linkage. These norbornene-based monomers were polymerized by a ring-opening metathesis polymerization initiated by a ruthenium-carbene complex (Grubbs catalyst) or a ruthenium-vinylidene complex. With a few exceptions, the polymers were soluble in THF, and casting the solution produced films. Solid-state hydrolysis of the estrone-conjugated polymer film showed a slow but steady release of estrone under mild conditions (pH 5.5 or 3.0 at 37 degrees C). (C) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.reactfunctpolym.2010.05.008
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文献信息

  • Ring-opening metathesis polymerization of steroid-conjugated norbornenes and gradual release of estrone from a polymer film
    作者:Shoujiro Ogawa、Shigenaga Takano、Hiroki Fujimori、Toshihiro Itoh、Shojiro Kaita、Takashi Iida、Yasuo Wakatsuki
    DOI:10.1016/j.reactfunctpolym.2010.05.008
    日期:2010.9
    Steroids (estrone, estradiol, ursodeoxycholic acid, chenodeoxycholic acid, cortisone, prednisone, and dexamethasone) were reacted with either 5-norbornene-2-carboxylic acid chloride or 5-norbornene-2-methanol to form new norbornene derivatives with bioactive and sterically demanding steroid residues bound with an ester linkage. These norbornene-based monomers were polymerized by a ring-opening metathesis polymerization initiated by a ruthenium-carbene complex (Grubbs catalyst) or a ruthenium-vinylidene complex. With a few exceptions, the polymers were soluble in THF, and casting the solution produced films. Solid-state hydrolysis of the estrone-conjugated polymer film showed a slow but steady release of estrone under mild conditions (pH 5.5 or 3.0 at 37 degrees C). (C) 2010 Elsevier Ltd. All rights reserved.
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