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4-Aza-1-azoniabicyclo[2.2.2]octane, 1-butyl- | 108203-98-1

中文名称
——
中文别名
——
英文名称
4-Aza-1-azoniabicyclo[2.2.2]octane, 1-butyl-
英文别名
1-butyl-4-aza-1-azoniabicyclo[2.2.2]octane
4-Aza-1-azoniabicyclo[2.2.2]octane, 1-butyl-化学式
CAS
108203-98-1
化学式
C10H21N2
mdl
——
分子量
169.29
InChiKey
KVUODFDAGLVVFI-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):
    1.1
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    3.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Molecular Design of Artificial Ribonucleases Using Electrostatic Interaction
    摘要:
    A number of small organic ribonucleases have been synthesized with rigid polycationic structures containing an aromatic framework with two residues of bisquaternary salts of 1,4-diazabicyclo [2.2.2] octane (DABCO) bearing various substituents. The compounds carrying positively charged groups connected via rigid linker are expected to bend the sugar-phosphate backbone and can stimulate the intramolecular phosphoester transfer reaction.
    DOI:
    10.1081/ncn-200026040
  • 作为产物:
    描述:
    三乙烯二胺 、 alkaline earth salt of/the/ methylsulfuric acid 以 丙酮 为溶剂, 生成 4-Aza-1-azoniabicyclo[2.2.2]octane, 1-butyl-
    参考文献:
    名称:
    Molecular Design of Artificial Ribonucleases Using Electrostatic Interaction
    摘要:
    A number of small organic ribonucleases have been synthesized with rigid polycationic structures containing an aromatic framework with two residues of bisquaternary salts of 1,4-diazabicyclo [2.2.2] octane (DABCO) bearing various substituents. The compounds carrying positively charged groups connected via rigid linker are expected to bend the sugar-phosphate backbone and can stimulate the intramolecular phosphoester transfer reaction.
    DOI:
    10.1081/ncn-200026040
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文献信息

  • PRODUCTION METHOD OF CARBAMIC ACID ESTER
    申请人:NATIONAL INSTITUTE OF ADVANCED INDUSTRIAL SCIENCE AND TECHNOLOGY
    公开号:US20190185420A1
    公开(公告)日:2019-06-20
    A method of production of carbamic acid ester has a high yield and high selectivity and is superior in economy. The method of production of a carbamic acid ester includes reacting an amine, carbon dioxide, and an alkoxysilane compound in the presence of a catalyst containing a zinc compound or an alkali metal compound or in the presence of an ionic liquid. A carbamic acid ester is produced, for example by reacting aniline, carbon dioxide, and tetramethoxysilane at a temperature of 150 to 180° C. in the presence of zinc acetate and 2,2′-bipyridine.
    一种生产氨基甲酸酯的方法具有高产率和高选择性,并在经济上优越。生产氨基甲酸酯的方法包括在催化剂的存在下,将胺、二氧化碳和烷氧基硅烷化合物反应,所述催化剂含有锌化合物或碱金属化合物或存在于离子液体中。例如,通过在150至180°C的温度下,在锌醋酸和2,2'-联吡啶的存在下,将苯胺、二氧化碳和四甲氧基硅烷反应,可以生产氨基甲酸酯。
  • Novel benzothiazepine and bensothiepine compounds
    申请人:Sasahara Takehiko
    公开号:US20070190041A1
    公开(公告)日:2007-08-16
    A pharmaceutical useful as a therapeutic agent and a preventive agent for hyperlipemia, and a pharmaceutical useful as a therapeutic agent and a preventive agent for hepatic disorders associated with cholestasis, particularly, primary biliary cirrhosis and primary sclerosing cholangitis, and a pharmaceutical useful as a therapeutic agent and a preventive agent for obesity, fatty liver and steatohepatitis are provided. A benzothiazepine or benzothiepine compound represented by the following formula (1A) having a thioamide bond and a quaternary ammonium substitutent:
    提供了一种药物,可用作治疗和预防高脂血症的治疗剂和预防剂,以及一种药物,可用作治疗和预防与胆汁淤积有关的肝脏疾病,特别是原发性胆汁性肝硬化和原发性硬化性胆管炎的治疗剂和预防剂,以及一种药物,可用作治疗和预防肥胖症、脂肪肝和脂肪性肝炎的治疗剂和预防剂。化合物的苯并噻吩或苯并噻环代表如下式(1A),具有硫酰胺键和季铵取代基:
  • Novel quaternary ammonium compounds
    申请人:Sasahara Takehiko
    公开号:US20070203115A1
    公开(公告)日:2007-08-30
    A method for inhibiting ileal bile acid transporter activity in a subject, comprising administering to said subject an effective amount of a compound represented by formula (1):
    一种抑制回肠胆汁酸转运蛋白活性的方法,包括向该受试者施用一种由式(1)所代表的化合物的有效量:
  • NOVEL BENZOTHIAZEPINE AND BENZOTHIEPINE COMPOUNDS
    申请人:SASAHARA Takehiko
    公开号:US20120015925A1
    公开(公告)日:2012-01-19
    A pharmaceutical useful as a therapeutic agent and a preventive agent for hyperlipemia, and a pharmaceutical useful as a therapeutic agent and a preventive agent for hepatic disorders associated with cholestasis, particularly, primary biliary cirrhosis and primary sclerosing cholangitis, and a pharmaceutical useful as a therapeutic agent and a preventive agent for obesity, fatty liver and steatohepatitis are provided. A benzothiazepine or benzothiepine compound represented by the following formula (1A) having a thioamide bond and a quaternary ammonium substituent:
    提供了一种作为治疗剂和预防剂用于高脂血症的药物,以及一种作为治疗剂和预防剂用于与胆汁淤积相关的肝疾病,特别是原发性胆汁性肝硬化和原发性硬化性胆管炎的药物,以及一种作为治疗剂和预防剂用于肥胖症、脂肪肝和脂肪性肝炎的药物。该药物是一种具有硫酰胺键和季铵基取代基的苯并噻吩或苯并噻吩化合物,其化学式为(1A)。
  • Method for manufacturing stabilized polyacetal resin, stabilized polyacetal resin, stabilized polyacetal resin composition, and molded article of stabilized polyacetal resin
    申请人:Polyplastics Co., Ltd.
    公开号:EP1867667A1
    公开(公告)日:2007-12-19
    The present invention provides an agent to decompose unstable terminal group, which is effective in a small adding amount, which sufficiently decreases the quantity of residual unstable terminal group, and which generates very little limitation on the treatment method, the apparatus, and the use amount of the agent. Specifically, it provides a method for manufacturing stabilized polyacetal resin having the step of applying heat treatment to a polyacetal resin having an unstable terminal group in the presence of an agent to decompose the unstable terminal group, which agent is composed of a heterocyclic quaternary ammonium salt, thus decreasing the quantity of the unstable terminal group.
    本发明提供了一种分解不稳定末端基团的药剂,其添加量小,效果好,能充分减少残留的不稳定末端基团的数量,并且对处理方法、装置和药剂的使用量限制很小。具体地说,它提供了一种制造稳定聚缩醛树脂的方法,该方法的步骤是:在有药剂存在的情况下,对具有不稳定末端基团的聚缩醛树脂进行热处理,以分解不稳定末端基团,该药剂由杂环季铵盐组成,从而减少不稳定末端基团的数量。
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