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N,N'-dimesityl-propane-1,3-diamine | 690662-85-2

中文名称
——
中文别名
——
英文名称
N,N'-dimesityl-propane-1,3-diamine
英文别名
N,N'-dimesitylpropane-1,3-diamine;N,N-dimesitylpropanediamine;1,3-Propanediamine, N,N'-bis(2,4,6-trimethylphenyl)-;N,N'-bis(2,4,6-trimethylphenyl)propane-1,3-diamine
N,N'-dimesityl-propane-1,3-diamine化学式
CAS
690662-85-2
化学式
C21H30N2
mdl
——
分子量
310.483
InChiKey
KJGQLDIMFGWGEX-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):
    6.1
  • 重原子数:
    23
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.43
  • 拓扑面积:
    24.1
  • 氢给体数:
    2
  • 氢受体数:
    2

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:
    参考文献:
    名称:
    1,3-二烷基和1,3-二芳基-3,4,5,6-四氢嘧啶-2-亚甲基铑(i)和钯(II)配合物:合成,结构和反应活性。
    摘要:
    描述了新型的1,3-二芳基和1,3-二烷基嘧啶-2-亚烷基的N-杂环卡宾(NHC)及其铑(i)和钯(II)配合物的合成。铑化合物溴(cod)[1,3-双(2-丙基)-3,4,5,6-四氢嘧啶-2-亚基]铑(7),溴(鳕鱼)(1,3-dimesityl-3 ,4,5,6-四氢嘧啶-2-亚基)铑(8)(cod = eta(4)-1,5-环辛二烯,均三= 2,4,6-三甲基苯基),氯(cod)(1,3 -dimesityl-3,4,5,6-四氢嘧啶-2-亚丙基)铑(9)和氯代(cod)[1,3-双(2-丙基)-3,4,5,6-四氢嘧啶-2 -[Yh(cod)Cl](2)]与叔丁醇锂反应,然后加入1,3-二甲硅烷基-1,3,4,5,6-四氢嘧啶溴化铵(10)制备亚吡啶基铑(10) 3),1,3-二甲磺酰基-1,3,4,5,6-四氢嘧啶四氟硼酸酯(4),1,3-二-2-丙基-3,4,5,6-四氢嘧啶溴化铵(6),和分别为1
    DOI:
    10.1002/chem.200305437
  • 作为产物:
    描述:
    2-溴-1,3,5-三甲基苯1,3-丙二胺 在 tris(dibenzylideneacetone)dipalladium (0) 、 R-(+)-1,1'-联萘-2,2'-双二苯膦 sodium t-butanolate 作用下, 以 甲苯 为溶剂, 140.0 ℃ 、10.0 MPa 条件下, 反应 70.0h, 以80%的产率得到N,N'-dimesityl-propane-1,3-diamine
    参考文献:
    名称:
    First silver complexes of tetrahydropyrimid-2-ylidenes
    摘要:
    The syntheses and characterizations of homoleptic silver(I) carbene complexes of the type LAgCl (3) and [L2Ag](2)(+)[Pd2Cl6](2-) (4) (L = dime sityltetrahyd ropyrimid-2-ylidene) are described. 3 was obtained by reaction of the corresponding tetrahydropyrimidinium salt with silver(I) oxide. Subsequent reaction of 3 with Pd(CH3CN)(2)Cl-2 afforded complex 4. The crystal structure of 3 has been determined to be a monomer in the solid state. The C-13 NMR spectra of both 3 and 4 exhibit C-13-Ag-107,Ag-109 coupling in solution. Furthermore, both compounds show a downfield shift of the carbene carbon of about 20 ppm to about 205 ppm in the C-13 NMR compared to five-membered ring silver(I) carbene complexes. Unlike other silver-carbene complexes, 3 does not undergo ligand exchange and can thus not be used for carbene transfer to other metals. (C) 2004 Elsevier B.V. All rights reserved.
    DOI:
    10.1016/j.jorganchem.2004.04.032
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文献信息

  • 1,3-Dialkyl- and 1,3-Diaryl-3,4,5,6-tetrahydropyrimidin-2-ylidene Rhodium(i) and Palladium(II) Complexes: Synthesis, Structure, and Reactivity
    作者:Monika Mayr、Klaus Wurst、Karl-Hans Ongania、Michael R. Buchmeiser
    DOI:10.1002/chem.200305437
    日期:2004.3.5
    respectively. Complex 7 crystallizes in the monoclinic space group P2(1)/n, and 8 in the monoclinic space group P2(1). Complexes 9 and 10 were used for the synthesis of the corresponding dicarbonyl complexes dicarbonylchloro(1,3-dimesityl-3,4,5,6-tetrahydropyrimidin-2-ylidene)rhodium (11), and dicarbonylchloro[1,3-bis(2-propyl)-3,4,5,6-tetrahydropyrimidin-2-ylidene]rhodium (12). The wavenumbers nu(CO I)/nu(CO
    描述了新型的1,3-二芳基和1,3-二烷基嘧啶-2-亚烷基的N-杂环卡宾(NHC)及其铑(i)和钯(II)配合物的合成。铑化合物溴(cod)[1,3-双(2-丙基)-3,4,5,6-四氢嘧啶-2-亚基]铑(7),溴(鳕鱼)(1,3-dimesityl-3 ,4,5,6-四氢嘧啶-2-亚基)铑(8)(cod = eta(4)-1,5-环辛二烯,均三= 2,4,6-三甲基苯基),氯(cod)(1,3 -dimesityl-3,4,5,6-四氢嘧啶-2-亚丙基)铑(9)和氯代(cod)[1,3-双(2-丙基)-3,4,5,6-四氢嘧啶-2 -[Yh(cod)Cl](2)]与叔丁醇锂反应,然后加入1,3-二甲硅烷基-1,3,4,5,6-四氢嘧啶溴化铵(10)制备亚吡啶基铑(10) 3),1,3-二甲磺酰基-1,3,4,5,6-四氢嘧啶四氟硼酸酯(4),1,3-二-2-丙基-3,4,5,6-四氢嘧啶溴化铵(6),和分别为1
  • Catalyst component for olefin polymerization
    申请人:Xu Guangxue
    公开号:US20050009690A1
    公开(公告)日:2005-01-13
    A solid catalyst component useful for the (co)-polymerization of olefins is disclosed. The catalyst component is prepared by reacting an activated magnesium halide composite support with a halogenized transition metal compound and a chelating diamide compound in the presence of organo-magnesium as a promoting agent and halogenized silicon or boron compounds as an activator. The catalyst component can be used with an organo-aluminum compound to provide a solid catalyst system that is compatible with slurry and gas phase polymerization processes. Linear low density polyethylene (LLDPE) produced using the catalyst component of the present invention displays a low molecular weight distribution, improved co-monomer incorporation, low content of the low molecular weight component, and excellent morphological properties such as spherical shape and high bulk density.
    本发明公开了一种用于烯烃(共)聚合的固体催化剂组分。该催化剂组分是在有机镁作为促进剂和卤化硅或硼化合物作为活化剂的存在下,通过活化卤化镁复合载体与卤化过渡金属化合物和螯合二酰胺化合物反应制备的。催化剂组分可与有机铝化合物一起使用,以提供一种与浆料和气相聚合工艺兼容的固体催化剂体系。使用本发明的催化剂组分生产的线性低密度聚乙烯(LLDPE)具有分子量分布低、共聚单体掺合度提高、低分子量组分含量低以及球形和高体积密度等优异的形态特性。
  • Paulsen, Andreas L.; Madsen, Robert, Heterocycles, 2004, vol. 63, # 9, p. 2051 - 2056
    作者:Paulsen, Andreas L.、Madsen, Robert
    DOI:——
    日期:——
  • US6992034B2
    申请人:——
    公开号:US6992034B2
    公开(公告)日:2006-01-31
  • First silver complexes of tetrahydropyrimid-2-ylidenes
    作者:Wolfgang A. Herrmann、Sabine K. Schneider、Karl Öfele、Masato Sakamoto、Eberhardt Herdtweck
    DOI:10.1016/j.jorganchem.2004.04.032
    日期:2004.8
    The syntheses and characterizations of homoleptic silver(I) carbene complexes of the type LAgCl (3) and [L2Ag](2)(+)[Pd2Cl6](2-) (4) (L = dime sityltetrahyd ropyrimid-2-ylidene) are described. 3 was obtained by reaction of the corresponding tetrahydropyrimidinium salt with silver(I) oxide. Subsequent reaction of 3 with Pd(CH3CN)(2)Cl-2 afforded complex 4. The crystal structure of 3 has been determined to be a monomer in the solid state. The C-13 NMR spectra of both 3 and 4 exhibit C-13-Ag-107,Ag-109 coupling in solution. Furthermore, both compounds show a downfield shift of the carbene carbon of about 20 ppm to about 205 ppm in the C-13 NMR compared to five-membered ring silver(I) carbene complexes. Unlike other silver-carbene complexes, 3 does not undergo ligand exchange and can thus not be used for carbene transfer to other metals. (C) 2004 Elsevier B.V. All rights reserved.
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