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3-hydroxy-2,2-dimethylcyclohexanone | 61447-86-7

中文名称
——
中文别名
——
英文名称
3-hydroxy-2,2-dimethylcyclohexanone
英文别名
3-Hydroxy-2,2-dimethylcyclohexan-1-one
3-hydroxy-2,2-dimethylcyclohexanone化学式
CAS
61447-86-7
化学式
C8H14O2
mdl
MFCD24390311
分子量
142.198
InChiKey
MAGFJLNBFXFQGX-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):
    0.7
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.875
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:cbb418af23a6921f74e9f3a71481e29b
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反应信息

  • 作为反应物:
    参考文献:
    名称:
    Barnier,J.-P.; Conia,J.-M., Bulletin de la Societe Chimique de France, 1975, p. 1654 - 1658
    摘要:
    DOI:
  • 作为产物:
    描述:
    2,2-二甲基-1,3-环己烷二酮甲醇 、 sodium tetrahydroborate 作用下, 反应 1.0h, 生成 3-hydroxy-2,2-dimethylcyclohexanone
    参考文献:
    名称:
    SUBSTITUTED DIAMINOPYRIMIDYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
    摘要:
    本文提供具有以下结构的二氨基嘧啶化合物: 其中X、L、R1和R2如本文所定义,包含有效量二氨基嘧啶化合物的组合物,以及用于治疗或预防PKC-theta介导的疾病或通过抑制激酶(例如PKC-theta)可治疗或预防的疾病的方法。
    公开号:
    US20150175557A1
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文献信息

  • SUBSTITUTED DIAMINOPYRIMIDYL COMPOUNDS, COMPOSITIONS THEREOF, AND METHODS OF TREATMENT THEREWITH
    申请人:Signal Pharmaceuticals, LLC
    公开号:US20150175557A1
    公开(公告)日:2015-06-25
    Provided herein are diaminopyrimidyl Compounds having the following structures: wherein X, L, R 1 , and R 2 are as defined herein, compositions comprising an effective amount of a Diaminopyrimidyl Compound, and methods for treating or preventing PKC-theta-mediated disorders, or a condition treatable or preventable by inhibition of a kinase, for example, PKC-theta.
    本文提供具有以下结构的二氨基嘧啶化合物: 其中X、L、R1和R2如本文所定义,包含有效量二氨基嘧啶化合物的组合物,以及用于治疗或预防PKC-theta介导的疾病或通过抑制激酶(例如PKC-theta)可治疗或预防的疾病的方法。
  • An NMR tool for cyclodextrin selection in enantiomeric resolution by high-performance liquid chromatography
    作者:Antonio Laverde、Gelson J. A. da Conceição、Sonia C. N. Queiroz、Fred Y. Fujiwara、Anita J. Marsaioli
    DOI:10.1002/mrc.1043
    日期:2002.7
    Complexation-induced chemical shifts and diffusion coefficients (HR-DOSY) of enantiomers with native and derivatized cyclodextrins were used for calculations of the apparent binding constants of three cyclohexanone inclusion complexes. Correlations between these data and high-performance liquid chromatography were established, revealing that this approach can be applied as an alternative method to predict enantiomeric discrimination. Copyright © 2002 John Wiley & Sons, Ltd.
    原生和衍生环糊精与手性分子的络合诱导化学位移和扩散系数(HR-DOSY)被用于计算三种环己酮包合物表观结合常数。通过这些数据与高效液相色谱之间的关联,揭示了该方法可作为预测手性识别的替代手段。版权© 2002 John Wiley & Sons, Ltd.
  • A Negishi cross-coupling reaction enables the total synthesis of (+)-stachyflin
    作者:Franz-Lucas Haut、Klaus Speck、Raphael Wildermuth、Kristof Möller、Peter Mayer、Thomas Magauer
    DOI:10.1016/j.tet.2018.02.048
    日期:2018.6
    present a full account on the development of the total synthesis of the antiviral meroterpenoid (+)-stachyflin. The decalin subunit is rapidly accessed by an exo-selective Diels–Alder reaction, whereas the isonindolinone was synthesized via a highly efficient and practical de novo route starting from dimedone. A challenging sp2–sp3 Negishi cross-coupling reaction enabled construction of the crucial C15–C16
    我们目前就抗病毒类萜(+)-水苏木素的全合成的发展提出了一个完整的说明。的萘烷亚基正在迅速由被访问的外切-选择性狄尔斯-阿尔德反应,而isonindolinone合成通过一高效实用的从头航线从双甲酮开始。具有挑战性的sp 2 –sp 3 Negishi交叉偶联反应使连接芳烃和萘烷亚单位的关键C15–C16键得以构建。为了最终安装顺式-十氢萘骨架,使用了路易斯酸催化的环化反应。
  • Synthesis of (+)-baiyunol, the diterpene aglycone of the sweet glycoside baiyunoside
    作者:Kenji Mori、Nakoto Komatsu
    DOI:10.1016/s0040-4020(01)81631-8
    日期:1987.1
    A chiral synthesis of (+)-baiyunol, the labdane-type diterpene aglycone of the sweet glycoside baiyunoside, was achieved starting from (S)-3-hydroxy-2,2-dimethylcyclohexanone.
    从(S)-3-羟基-2,2-二甲基环己酮开始,实现了(+)-baiyunol的手性合成,这是甜糖苷baiyunoside的拉丹烷型二萜糖苷。
  • Substituted diaminopyrimidyl compounds, compositions thereof, and methods of treatment therewith
    申请人:Signal Pharmaceuticals, LLC
    公开号:US09156798B2
    公开(公告)日:2015-10-13
    Provided herein are diaminopyrimidyl Compounds having the following structures: wherein X, L, R1, and R2 are as defined herein, compositions comprising an effective amount of a Diaminopyrimidyl Compound, and methods for treating or preventing PKC-theta-mediated disorders, or a condition treatable or preventable by inhibition of a kinase, for example, PKC-theta.
    本文提供了具有以下结构的二氨基嘧啶化合物:其中X,L,R1和R2如本文所定义,包含有效量的二氨基嘧啶化合物的组合物,以及用于治疗或预防PKC-theta介导的疾病或可通过抑制激酶(例如PKC-theta)治疗或预防的疾病的方法。
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