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(S)-cyclohex-3-en-1-yl methanesulfonate | 290310-93-9

中文名称
——
中文别名
——
英文名称
(S)-cyclohex-3-en-1-yl methanesulfonate
英文别名
[(1S)-cyclohex-3-en-1-yl]methyl methanesulfonate
(S)-cyclohex-3-en-1-yl methanesulfonate化学式
CAS
290310-93-9
化学式
C8H14O3S
mdl
——
分子量
190.263
InChiKey
DRPKJZBPDGBVJF-MRVPVSSYSA-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):
    1.32
  • 重原子数:
    12.0
  • 可旋转键数:
    3.0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    43.37
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

  • 作为反应物:
    描述:
    (S)-cyclohex-3-en-1-yl methanesulfonate 在 Raney-Cu 作用下, 以 二甲基亚砜 为溶剂, 反应 18.5h, 生成 (1S)-cyclohex-3-eneacetamide
    参考文献:
    名称:
    摘要:
    Cyclic nucreo-delta-amino acids that constitute monomers of a conformationally constrained nucleo-delta-peptide base-pairing system have been prepared. Their synthesis starts with an enantioselectively catalyzed chirogenic Diels-Alder reaction, proceeds via a regioselective epsilon-iodolactamization process, and ends with a regio- as well as diastereoselective introduction of nucleobases through S(N)2-type opening of a transiently formed N-acylaziridine ring. Extensive use of X-ray crystal-structure analysis has been made to support structure assignments.
    DOI:
    10.1002/1522-2675(20000607)83:6<1049::aid-hlca1049>3.0.co;2-1
  • 作为产物:
    描述:
    methyl (1S)-cyclohex-3-ene-1-carboxylate 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃吡啶 为溶剂, 反应 3.5h, 生成 (S)-cyclohex-3-en-1-yl methanesulfonate
    参考文献:
    名称:
    摘要:
    Cyclic nucreo-delta-amino acids that constitute monomers of a conformationally constrained nucleo-delta-peptide base-pairing system have been prepared. Their synthesis starts with an enantioselectively catalyzed chirogenic Diels-Alder reaction, proceeds via a regioselective epsilon-iodolactamization process, and ends with a regio- as well as diastereoselective introduction of nucleobases through S(N)2-type opening of a transiently formed N-acylaziridine ring. Extensive use of X-ray crystal-structure analysis has been made to support structure assignments.
    DOI:
    10.1002/1522-2675(20000607)83:6<1049::aid-hlca1049>3.0.co;2-1
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