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(2R)-3-tolyloxy-1,2-propanediol acetonide | 52094-00-5

中文名称
——
中文别名
——
英文名称
(2R)-3-tolyloxy-1,2-propanediol acetonide
英文别名
(2R)-3-o-Tolyloxy-1,2-propandiolacetonid;(4R)-2,2-Dimethyl-4-[(2-methylphenoxy)methyl]-1,3-dioxolane;(4R)-2,2-dimethyl-4-[(2-methylphenoxy)methyl]-1,3-dioxolane
(2R)-3-tolyloxy-1,2-propanediol acetonide化学式
CAS
52094-00-5
化学式
C13H18O3
mdl
——
分子量
222.284
InChiKey
VWYJFDMNXJTNQS-LLVKDONJSA-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:
    298.3±20.0 °C(Predicted)
  • 密度:
    1.034±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.5
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.54
  • 拓扑面积:
    27.7
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:29cabc3afab52a359ad00c06dd6a75a0
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上下游信息

  • 下游产品
    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:
    参考文献:
    名称:
    3-芳氧基丙烷-1,2-二醇及其衍生物的绝对构型:美信素异构体
    摘要:
    由2 R-和2 S -3-甲苯磺酰氧基丙烷-1,2-二醇丙酮化物与邻甲酚(NaOH)反应制得美芬素(3-邻甲苯基丙烷-1,2-二醇)的旋光异构体根据Cupra A解决方案中的cd光谱确定。
    DOI:
    10.1039/c39730000896
  • 作为产物:
    描述:
    邻甲酚(R)-(-)-甘油醇缩丙酮三苯基膦偶氮二甲酸二乙酯 作用下, 以 四氢呋喃 为溶剂, 反应 12.0h, 以52%的产率得到(2R)-3-tolyloxy-1,2-propanediol acetonide
    参考文献:
    名称:
    Cardiovascular hybrid drugs: new benzazepinone derivatives as bradycardic agents endowed with selective β 1 -Non-competitive antagonism
    摘要:
    The synthesis and pharmacological profile of some hybrid compounds bearing both the benzazepinone moiety present in Zatebradine and typical P-blocker aryloxypropanolamine groups are described. The new compounds proved to be endowed with negative chronotropic and inotropic activity and are weak vasorelaxant agents. The cardiodepressant action is probably due to selective beta(1)-noncompetitive reversible antagonism. Both enantiomers of the most active compound 5c were synthesized and they showed a different cardiovascular profile, that is (+)-(R)-enantiomer displays affinity for cardiac beta(1)-adrenoceptors, while (-)-(S)-enantiomer shows specificity for vessel smooth muscle. (C) 2003 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(02)00621-1
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文献信息

  • Absolute configuration of glycerol derivatives. 3. Synthesis and Cupra A circular dichroism spectra of some chiral 3-aryloxy-1,2-propanediols and 3-aryloxy-1-amino-2-propanols
    作者:Wendel L. Nelson、John E. Wennerstrom、S. Raman Sankar
    DOI:10.1021/jo00426a016
    日期:1977.3
  • Cardiovascular hybrid drugs: new benzazepinone derivatives as bradycardic agents endowed with selective β 1 -Non-competitive antagonism
    作者:Alessandra Bisi、Angela Rampa、Roberta Budriesi、Silvia Gobbi、Federica Belluti、Pierfranco Ioan、Ermanno Valoti、Alberto Chiarini、Piero Valenti
    DOI:10.1016/s0968-0896(02)00621-1
    日期:2003.4
    The synthesis and pharmacological profile of some hybrid compounds bearing both the benzazepinone moiety present in Zatebradine and typical P-blocker aryloxypropanolamine groups are described. The new compounds proved to be endowed with negative chronotropic and inotropic activity and are weak vasorelaxant agents. The cardiodepressant action is probably due to selective beta(1)-noncompetitive reversible antagonism. Both enantiomers of the most active compound 5c were synthesized and they showed a different cardiovascular profile, that is (+)-(R)-enantiomer displays affinity for cardiac beta(1)-adrenoceptors, while (-)-(S)-enantiomer shows specificity for vessel smooth muscle. (C) 2003 Elsevier Science Ltd. All rights reserved.
  • Absolute configuration of 3-aryloxypropane-1,2-diols and derivatives: mephenesin isomers
    作者:Wendel L. Nelson、Carl E. Wood
    DOI:10.1039/c39730000896
    日期:——
    The optical isomers of mephenesin (3-o-tolylpropane-1,2-diol) were prepared from 2R- and 2S-3-tosyloxypropane-1,2-diol acetonide by reaction with o-cresol(NaOH) and the configurations confirmed on the basis of c.d. spectra in Cupra A Solution.
    由2 R-和2 S -3-甲苯磺酰氧基丙烷-1,2-二醇丙酮化物与邻甲酚(NaOH)反应制得美芬素(3-邻甲苯基丙烷-1,2-二醇)的旋光异构体根据Cupra A解决方案中的cd光谱确定。
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