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N-isopropyl-N-2-(1-oxocyclo-hex-2-enyl)cyclohexanecarboxamide | 93831-71-1

中文名称
——
中文别名
——
英文名称
N-isopropyl-N-2-(1-oxocyclo-hex-2-enyl)cyclohexanecarboxamide
英文别名
N-isopropyl-N-2-(1-oxocyclohex-2-enyl)-cyclohexanecarboxamide;N-isopropyl-N-2-(1-oxocyclohex-2-enyl)cyclohexanecarboxamide;N-(6-oxocyclohexen-1-yl)-N-propan-2-ylcyclohexanecarboxamide
N-isopropyl-N-2-(1-oxocyclo-hex-2-enyl)cyclohexanecarboxamide化学式
CAS
93831-71-1
化学式
C16H25NO2
mdl
——
分子量
263.38
InChiKey
PPZCWILIMCSIQQ-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

物化性质

  • 沸点:
    436.2±35.0 °C(Predicted)
  • 密度:
    1.05±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    19
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    37.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

点击查看最新优质反应信息

文献信息

  • Enantioselective Photocyclization of Amides to β-Lactam Derivatives in Inclusion Crystals with an Optically Active Host
    作者:Fumio Toda、Hisakazu Miyamoto、Mitsuhiro Inoue、Shunpei Yasaka、Ivanka Matijasic
    DOI:10.1021/jo991832m
    日期:2000.5.1
    Irradiation of inclusion crystals of 2-(N-acyl-N-alkylamino)cyclohex-2-enones and N,N-dimethylphenylglyoxylamide with chiral host molecules gave the optically active N-alkyl-1-azaspiro[3.5]-nonane-2,5-diones and 3-hydroxy-1-methyl-3-phenylazetidin-2-one, respectively. The crystal structure of the 1:1 inclusion complex of N,N-dimethylphenylglyoxylamide with (-)-trans-1,4-bis[3-(o-chlorophenyl)-3-hy
    用手性主体分子辐照2-(N-酰基-N-烷基基)环己-2-烯酮和N,N-二甲基苯基乙醛酰胺的包裹体晶体,得到旋光性的N-烷基-1-氮杂螺[3.5]-壬烷-2, 5-二酮和3-羟基-1-甲基-3-苯基氮杂环丁烷-2-一。N,N-二甲基苯基乙醛酰胺与(-)-反式-1,4-双[3-(邻氯苯基)-3-羟基-3-苯基丙-1-炔基]-的1:1包合物的晶体结构通过X射线衍射分析2,3,5,6-四-2,5-环己二烯-1,4-二醇
  • Designs of host/guest molecular and crystal structures
    作者:Fumio Toda
    DOI:10.1016/0022-2860(95)09090-8
    日期:1996.1
    Abstract When an optically active host compound was mixed with an achiral guest compound in the solid state, host-guest inclusion crystals were formed by molecular movement and the achiral molecules became arranged in a chiral form in the inclusion crystals.
    摘要 当光学活性主体化合物与固态非手性客体化合物混合时,通过分子运动形成主客体包合物,非手性分子在包合物中以手性形式排列。
  • Achiral Molecules Move and Order Themselves in a Chiral Form in Host-Guest Inclusion Crystals
    作者:Fumio Toda、Hisakazu Miyamoto
    DOI:10.1246/cl.1995.809
    日期:1995.9
    When optically active host compound was mixed with achiral guest compound in the solid state, host-guest inclusion crystals were formed by molecular movement and the achiral molecules became arranged in a chiral form in the inclusion crystals. Mixing of powdered (+)-host crystals with powdered (−)-guest crystals which are formed by a chiral arrangement of achiral guest molecules gave inclusion crystals of the (+)-host and the (+)-guest molecules newly produced through an inversion of the (−)-guest molecules during the complexation in the solid state.
    当光学活性主化合物与非手性客体化合物在固态下混合时,通过分子运动形成了主-客体包晶,非手性分子在包晶中呈手性排列。将粉末状(+)-主晶与粉末状(-)-客晶混合,后者是由非手性客体分子的手性排列形成的,在固态络合过程中,通过(-)-客体分子的反转,产生了新的(+)-主晶和(+)-客体分子的包合物晶体。
  • Miyamoto, Hisakazu; Kikuchi, Siro; Oki, Yasuo, Molecular Crystals and Liquid Crystals Science and Technology, Section A: Molecular Crystals and Liquid Crystals, 1996, vol. 276-277, p. 73 - 78
    作者:Miyamoto, Hisakazu、Kikuchi, Siro、Oki, Yasuo、Inoue, Mitsuhiro、Kanemoto, Kazuyuki、Toda, Fumio
    DOI:——
    日期:——
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