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tert-butyl methyl(1-(((5-vinylpyridin-3-yl)oxy)methyl)cyclopropyl)carbamate | 959865-36-2

中文名称
——
中文别名
——
英文名称
tert-butyl methyl(1-(((5-vinylpyridin-3-yl)oxy)methyl)cyclopropyl)carbamate
英文别名
——
tert-butyl methyl(1-(((5-vinylpyridin-3-yl)oxy)methyl)cyclopropyl)carbamate化学式
CAS
959865-36-2
化学式
C17H24N2O3
mdl
——
分子量
304.389
InChiKey
ZTSNFHUOOFKDSW-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):
    3.5
  • 重原子数:
    22.0
  • 可旋转键数:
    5.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.53
  • 拓扑面积:
    51.66
  • 氢给体数:
    0.0
  • 氢受体数:
    4.0

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

反应信息

  • 作为反应物:
    描述:
    tert-butyl methyl(1-(((5-vinylpyridin-3-yl)oxy)methyl)cyclopropyl)carbamate盐酸 作用下, 以 1,4-二氧六环 为溶剂, 以65%的产率得到N-methyl-1-((5-vinylpyridin-3-yloxy)methyl)cyclopropanamine hydrochloride
    参考文献:
    名称:
    Preparation and affinity profile of novel nicotinic ligands
    摘要:
    Novel nicotinic ligands, characterized by the presence of an amino substituted cyclopropane ring connected to a pyridine nucleus, are described. Pharmacological investigation revealed that these compounds exhibit highest affinity for the rat alpha 4 beta 2 subtype of the nicotinic receptor with no affinity for the muscarinic receptor. No appreciable affinity for the muscular or for the ganglionic nicotinic receptor was observed at concentrations up to 10 mu M. The increase in cortical ACh release as well as a positive effect on memory in a social recognition test in rat are exemplified. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.12.075
  • 作为产物:
    描述:
    tert-butyl 1-([(5-bromopyridin-3-yl)oxy]methyl)cyclopropyl(methyl)carbamate三丁基乙烯基锡四(三苯基膦)钯 作用下, 以 甲苯 为溶剂, 以80%的产率得到tert-butyl methyl(1-(((5-vinylpyridin-3-yl)oxy)methyl)cyclopropyl)carbamate
    参考文献:
    名称:
    Preparation and affinity profile of novel nicotinic ligands
    摘要:
    Novel nicotinic ligands, characterized by the presence of an amino substituted cyclopropane ring connected to a pyridine nucleus, are described. Pharmacological investigation revealed that these compounds exhibit highest affinity for the rat alpha 4 beta 2 subtype of the nicotinic receptor with no affinity for the muscarinic receptor. No appreciable affinity for the muscular or for the ganglionic nicotinic receptor was observed at concentrations up to 10 mu M. The increase in cortical ACh release as well as a positive effect on memory in a social recognition test in rat are exemplified. (C) 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2007.12.075
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