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[1-(Benzenesulfonyl)piperidin-4-yl](phenyl)methanone | 922504-25-4

中文名称
——
中文别名
——
英文名称
[1-(Benzenesulfonyl)piperidin-4-yl](phenyl)methanone
英文别名
[1-(benzenesulfonyl)piperidin-4-yl]-phenylmethanone
[1-(Benzenesulfonyl)piperidin-4-yl](phenyl)methanone化学式
CAS
922504-25-4
化学式
C18H19NO3S
mdl
——
分子量
329.42
InChiKey
AFQYLZGGMHLKMO-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:
    497.7±55.0 °C(Predicted)
  • 密度:
    1.258±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    23
  • 可旋转键数:
    4
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.28
  • 拓扑面积:
    62.8
  • 氢给体数:
    0
  • 氢受体数:
    4

SDS

SDS:52150fec589fd68d5e45c044a28ab892
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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
  • 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:
    CAN-mediated rearrangement of 4-benzhydrylidenepiperidines
    摘要:
    Several 1-substituted phenyl-(4-phenylpiperidin-4-yl)methanones are synthesized in modest overall yields starting from the reaction of different 1-substituted 4-benzhydrylidenepiperidines via CAN-mediated rearrangement. This facile strategy was also used to synthesize meperidine analog. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2006.09.068
  • 作为产物:
    描述:
    (1-benzenesulfonyl-piperidin-4-yl)-methanol 在 Celite 、 pyridinium chlorochromate 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 生成 [1-(Benzenesulfonyl)piperidin-4-yl](phenyl)methanone
    参考文献:
    名称:
    Synthesis of diarylazepan-4-ones
    摘要:
    Synthesis of several 3,3-diarylazepan-4-ones and 5,5-diarylazepan-4-ones has been established starting from two tetrasubstituted olefins, which is derived from commercially available piperidine-3-carboxylic acid ethyl ester and piperidine-4-carboxylic acid ethyl ester. The single isomer with the structural skeleton of 3,3-diarylazepan-4-one and 5,5-diarylazepan-4-one is constructed in two functional group transformations of Grignard addition/dehydration and epoxidation/pinacol rearrangement. (c) 2006 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2006.11.072
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文献信息

  • Synthesis of diarylazepan-4-ones
    作者:Meng-Yang Chang、Yung-Hua Kung、Chih-Chong Ma
    DOI:10.1016/j.tetlet.2006.11.072
    日期:2007.1
    Synthesis of several 3,3-diarylazepan-4-ones and 5,5-diarylazepan-4-ones has been established starting from two tetrasubstituted olefins, which is derived from commercially available piperidine-3-carboxylic acid ethyl ester and piperidine-4-carboxylic acid ethyl ester. The single isomer with the structural skeleton of 3,3-diarylazepan-4-one and 5,5-diarylazepan-4-one is constructed in two functional group transformations of Grignard addition/dehydration and epoxidation/pinacol rearrangement. (c) 2006 Elsevier Ltd. All rights reserved.
  • CAN-mediated rearrangement of 4-benzhydrylidenepiperidines
    作者:Meng-Yang Chang、Tsun-Cheng Wu、Chun-Yu Lin、Ching-Yi Hung
    DOI:10.1016/j.tetlet.2006.09.068
    日期:2006.11
    Several 1-substituted phenyl-(4-phenylpiperidin-4-yl)methanones are synthesized in modest overall yields starting from the reaction of different 1-substituted 4-benzhydrylidenepiperidines via CAN-mediated rearrangement. This facile strategy was also used to synthesize meperidine analog. (c) 2006 Elsevier Ltd. All rights reserved.
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