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2-(2-丙氧基乙基)吡啶 | 70644-45-0

中文名称
2-(2-丙氧基乙基)吡啶
中文别名
——
英文名称
2-(2-propoxyethyl)pyridine
英文别名
——
2-(2-丙氧基乙基)吡啶化学式
CAS
70644-45-0
化学式
C10H15NO
mdl
MFCD00006363
分子量
165.235
InChiKey
ZLJMIUFTLBIOEK-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):
    1.6
  • 重原子数:
    12
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    22.1
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    3-丙氧基丙腈乙炔decamethylrhenocene 作用下, 以 甲苯 为溶剂, 以77%的产率得到2-(2-丙氧基乙基)吡啶
    参考文献:
    名称:
    Photocatalyzed [2 + 2 + 2]-Cycloaddition of Nitriles with Acetylene:  An Effective Method for the Synthesis of 2-Pyridines under Mild Conditions
    摘要:
    The photocatalyzed [2 + 2 + 2]-cycloaddition of nitriles with 2 equiv of acetylene to 2-pyridines can be carried out under mild conditions and represents a valuable extension to common synthetical methods. For the ideal wavelength range (350-500 nm), lamps as well as sunlight can be used. Working at room temperature and in organic solvents such as toluene or hexane as well as in water gives satisfying results in many cases. However, it is also possible to vary the solvent and the reaction temperature of the photocatalyzed synthesis and to choose, with respect to the specific substrate, specific requirements for this particular reaction and general requirements of the method. This simple and selective method derives its potential mainly from the large variety of applicable nitriles. Suitable substrates include (functionalized) aliphatic and aromatic nitriles as well as cyanamides derived from secondary amines.
    DOI:
    10.1021/jo011032n
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文献信息

  • Negative curable dye-containing composition, color filter, and method of manufacturing the same
    申请人:Takakuwa Hideki
    公开号:US20070072096A1
    公开(公告)日:2007-03-29
    The invention provides a negative curable dye-containing composition including at least one compound selected from amine and pyridine compounds, a phthalocyanine dye soluble in an organic solvent, a photopolymerization initiator, and a radical polymerizable monomer, a color filter formed by using the same, and a manufacturing method of the color filter.
  • Electrolyte Formulations
    申请人:KAWATA Kentaro
    公开号:US20120318360A1
    公开(公告)日:2012-12-20
    The present invention relates to electrolyte formulations comprising at least one imidazolium difluorodicyanoborate or pyrrolidinium difluorodicyanoborate and their use in an electrochemical and/or optoelectronic device such as a photovoltaic cell, a light emitting device, an electrochromic or photo-electrochromic device, an electrochemical sensor and/or biosensor, preferably their use in a dye or quantum dot-sensitized solar cell
  • US5939568A
    申请人:——
    公开号:US5939568A
    公开(公告)日:1999-08-17
  • US8829201B2
    申请人:——
    公开号:US8829201B2
    公开(公告)日:2014-09-09
  • [EN] ACCELERATED CATALYSIS OF OLEFINIC EPOXIDATIONS<br/>[FR] CATALYSE ACCELEREE DES EPOXYDATIONS OLEFINIQUES
    申请人:——
    公开号:WO1998033786A1
    公开(公告)日:1998-08-06
    [EN] Rhenium-catalyzed epoxidation of olefinic substrates is accelerated by the use of accelerants having a nitrogenous aromatic heterocyclic structure. Use of the accelerants also enables the use of aqueous hydrogen peroxide as an oxidant. To achieve optimum acceleration, the accelerant should have a concentration within a range from 2.0 mole percent to 100 mole percent of the accelerant with respect to 1 mole of the olefinic substrate. Use of the accelerant also results in an increased yield with respect to the conversion of the olefinic substrate to epoxide product.
    [FR] L'invention se rapporte à l'époxydation de substrats oléfiniques catalysée par le rhénium, qui est accélérée par des accélérateurs à structure hétérocyclique aromatique azotée. En outre, le recours à des accélérateurs permet d'utiliser en tant qu'oxydant le peroxyde d'hydrogène aqueux. Afin d'obtenir une accélération optimale, il faut que la concentration de l'accélérateur soit comprise comprise entre 2,0 et 100 moles d'accélérateur pour cent moles de substrat oléfinique. Le recours à l'accélérateur permet également d'assurer un rendement plus élevé en matière de conversion du substrat oléfinique en produit époxyde.
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