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2-[3-(二甲氨基)苯氧基]乙醇 | 1025914-75-3

中文名称
2-[3-(二甲氨基)苯氧基]乙醇
中文别名
——
英文名称
2-[3-(dimethylamino)phenoxy]ethanol
英文别名
2-(3-(Dimethylamino)phenoxy)ethanol
2-[3-(二甲氨基)苯氧基]乙醇化学式
CAS
1025914-75-3
化学式
C10H15NO2
mdl
——
分子量
181.235
InChiKey
MBYVSWLLXWATBW-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:
    297.0±15.0 °C(Predicted)
  • 密度:
    1.095±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    13
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.4
  • 拓扑面积:
    32.7
  • 氢给体数:
    1
  • 氢受体数:
    3

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:
    描述:
    4-硝基邻苯二甲腈2-[3-(二甲氨基)苯氧基]乙醇potassium carbonate 作用下, 以 N,N-二甲基甲酰胺 为溶剂, 反应 96.0h, 以50%的产率得到4-{2-[3-(dimethylamino)phenoxy]ethoxy}phthalonitrile
    参考文献:
    名称:
    带有可电聚合二甲胺基团的无金属和金属酞菁的合成,表征,电化学和光谱电化学性质
    摘要:
    新颖外周四的合成和表征取代的不含金属4和金属酞菁5 - 7是在本研究中首次描述。所有这些新化合物的特征是IR,1 H和13的组合核磁共振,质谱和紫外可见光谱技术。采用循环伏安法和方波伏安法研究了无金属,镍(II),钴(II)和铜(II)酞菁的电化学和光谱电化学性质。尽管所有络合物均具有通用的还原过程,但它们会在工作电极上发生电聚合。配合物的施加电势和金属中心的类型会影响电聚合机理。光谱电化学和电比色法测量表明,配合物的电产生的阴离子物质具有明显的色差,这是配合物电致变色应用的期望因素。
    DOI:
    10.1016/j.dyepig.2013.03.021
  • 作为产物:
    描述:
    3-羟基-N,N-二甲基苯胺2-氯乙醇 在 sodium hydroxide 作用下, 以 乙醇 为溶剂, 反应 21.5h, 以59%的产率得到2-[3-(二甲氨基)苯氧基]乙醇
    参考文献:
    名称:
    带有可电聚合二甲胺基团的无金属和金属酞菁的合成,表征,电化学和光谱电化学性质
    摘要:
    新颖外周四的合成和表征取代的不含金属4和金属酞菁5 - 7是在本研究中首次描述。所有这些新化合物的特征是IR,1 H和13的组合核磁共振,质谱和紫外可见光谱技术。采用循环伏安法和方波伏安法研究了无金属,镍(II),钴(II)和铜(II)酞菁的电化学和光谱电化学性质。尽管所有络合物均具有通用的还原过程,但它们会在工作电极上发生电聚合。配合物的施加电势和金属中心的类型会影响电聚合机理。光谱电化学和电比色法测量表明,配合物的电产生的阴离子物质具有明显的色差,这是配合物电致变色应用的期望因素。
    DOI:
    10.1016/j.dyepig.2013.03.021
  • 作为试剂:
    描述:
    sodium methylate 、 2-(3-(Dimethylamino)phenoxy)ethyl acetate 在 crude material 、 silica gel 、 乙酸乙酯2-[3-(二甲氨基)苯氧基]乙醇 作用下, 以 甲醇 为溶剂, 反应 2.5h, 以EtOAc 66:34-50:50, to provide the desired compound 2-(3-(dimethylamino)phenoxy)ethanol (39B)的产率得到2-[3-(二甲氨基)苯氧基]乙醇
    参考文献:
    名称:
    Compounds and methods of use
    摘要:
    在某个方面,本发明提供了一个I式化合物,其中在I式中,变量X1,X2a,X2b,X2c,R1,B,L,E,A和下标n的定义如本文所述。在另一个方面,本发明提供了包含I式化合物的药物组合物,以及使用I式化合物治疗表达或过度表达Bcl-2抗凋亡蛋白(例如抗凋亡Bcl-xL蛋白)所致的疾病和状况(例如癌症,血小板增多症等)的方法。
    公开号:
    US09067928B2
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文献信息

  • COMPOUNDS AND METHODS OF USE
    申请人:Baell Jonathan Bayldon
    公开号:US20100190782A1
    公开(公告)日:2010-07-29
    In one aspect, the present invention provides for a compound of Formula I in which in Formula I, the variables X 1 , X 2a , X 2b , X 2c , R 1 , B, L, E, A and the subscript n are as defined herein. In another aspect, the present invention provides for pharmaceutical compositions comprising compounds of Formula I as well as methods for using compounds of Formula I for the treatment of diseases and conditions (e.g., cancer, thrombocythemia, etc) characterized by the expression or over-expression of Bcl-2 anti-apoptotic proteins, e.g., of anti-apoptotic Bcl-x L proteins.
    在一个方面,本发明提供了一种I式化合物,其中在I式中,变量X1、X2a、X2b、X2c、R1、B、L、E、A和下标n的定义如本文所述。在另一个方面,本发明提供了包括I式化合物的制药组合物,以及使用I式化合物治疗疾病和病情(如癌症、血小板增多症等)的方法,其中这些疾病和病情的特征是Bcl-2抗凋亡蛋白的表达或过度表达,例如抗凋亡Bcl-xL蛋白。
  • New water soluble cationic zinc phthalocyanines as potential for photodynamic therapy of cancer
    作者:Dilek Çakır、Volkan Çakır、Zekeriya Bıyıklıoğlu、Mahmut Durmuş、Halit Kantekin
    DOI:10.1016/j.jorganchem.2013.08.025
    日期:2013.11
    The novel phthalonitrile derivatives (2 and 3) bearing 2-[3-(dimethylamino)phenoxy]ethanol sub-stituents on the 3 and 4 positions have been synthesized. The novel peripherally and non-peripherally tetra-2-[3-(dimethylamino)phenoxy]} substituted zinc phthalocyanines (2a and 3a) were also synthesized by cyclotetramerization of phthalonitrile derivatives (2 and 3). The obtained new zinc phthalocyanines (2a and 3a) were converted into water-soluble quaternized products (2b and 3b). The new compounds have been characterized by combination of spectroscopic data including UV-Vis, IR, H-1 NMR, C-13 NMR, MS spectroscopic data and elemental analysis as well. The photophysical and photochemical properties of newly synthesized zinc phthalocyanines were investigated in DMSO for non-ionic and in both DMSO and phosphate buffer solution (PBS) for ionic compounds. The obtained ionic complexes (2b, 3b) show excellent solubility in both organic and aqueous solutions which is very useful for the treatment of cancer by photodynamic therapy (PDT). (C) 2013 Elsevier B. V. All rights reserved.
  • Synthesis, characterization and investigation of homogeneous oxidation activities of peripherally tetra-substituted Co(II) and Fe(II) phthalocyanines: Oxidation of cyclohexene
    作者:Zekeriya Bıyıklıoğlu、Ece Tuğba Saka、Serpil Gökçe、Halit Kantekin
    DOI:10.1016/j.molcata.2013.06.009
    日期:2013.11
    The synthesis and characterization of novel peripherally tetra-substituted iron(II) 4 and cobalt(II) 5 phthalocyanines are described for the first time in this study. All the new compounds are characterized by a combination of IR, H-1 and C-13 NMR, mass and UV-vis spectroscopy techniques. Complexes 4 and 5 served as catalyst for the oxidation of cyclohexene using different types of oxidants, such as tert-butyl hydroperoxide (TBHP), m-chloroperoxybenzoic acid (m-CPBA), aerobic oxygen and hydrogen peroxide (H2O2). During the oxidation process the products formed are 2-cyclohexene-1-ol, 2-cyclohexene-1-one and cyclohexene oxide. The selectivity for 2-cyclohexene-1-ol is favored when iron(II) and cobalt(II) phthalocyanine catalysts are employed. The higher conversion is obtained as catalyst iron(II) phthalocyanine (96%). TBHP was determined as the successful oxidant with the minimum demolition of the catalyst, superior selectivity and conversion in the oxidation products. (c) 2013 Elsevier B.V. All rights reserved.
  • Azofarbstoffe, deren Herstellung und Verwendung
    申请人:CIBA-GEIGY AG
    公开号:EP0042357B1
    公开(公告)日:1984-06-06
  • LUBRICANT COMPOSITION, MECHANICAL ELEMENT, AND METHOD FOR PRODUCING TRIAZINE DERIVATIVES
    申请人:Negoro Masayuki
    公开号:US20080274920A1
    公开(公告)日:2008-11-06
    A lubricant composition comprising following ingredients (a) and (b) is disclosed. (a) at least one compound represented by formula (1) (b) at least one compound represented by formula (2) (R—X-) m -D   (1) (b) at least one compound represented by formula (2)
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