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(2,3-diamino-2,3-dimethylbutane)dichlorozinc(II) | 256398-64-8

中文名称
——
中文别名
——
英文名称
(2,3-diamino-2,3-dimethylbutane)dichlorozinc(II)
英文别名
Dichlorozinc;2,3-dimethylbutane-2,3-diamine
(2,3-diamino-2,3-dimethylbutane)dichlorozinc(II)化学式
CAS
256398-64-8
化学式
C6H16Cl2N2Zn
mdl
——
分子量
252.502
InChiKey
WLAYVESTYQFTAM-UHFFFAOYSA-L
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):
    1.84
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    52
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    2,3-二甲基-2,3-丁二胺(2,3-diamino-2,3-dimethylbutane)dichlorozinc(II)乙醚 为溶剂, 以60%的产率得到bis(2,3-diamino-2,3-dimethylbutane)aquazinc(II) chloride monohydrate
    参考文献:
    名称:
    Synthesis of vicinal bishydroxylamine
    摘要:
    Reduction of 2,3-dimethyl-2,3-dinitrobutane with Zn in aqueous ethanol in the presence of NH(4)Cl affords 2,3-bis(hydroxylamino)-2,3-dimethylbutane together with 2,3-diamino-2,3-dimethylbutane and complex Zn salts. A modified procedure was developed for the synthesis of bishydroxylamine, which involves reduction in a Zn/NH(4)Cl/THF-H(2)O system.
    DOI:
    10.1007/bf02496404
  • 作为产物:
    描述:
    2,3-dimethyl-2,3-butanediamine dihydrochloride 、 zinc(II) chloride 在 NaOH 作用下, 以 为溶剂, 以75%的产率得到(2,3-diamino-2,3-dimethylbutane)dichlorozinc(II)
    参考文献:
    名称:
    Synthesis of vicinal bishydroxylamine
    摘要:
    Reduction of 2,3-dimethyl-2,3-dinitrobutane with Zn in aqueous ethanol in the presence of NH(4)Cl affords 2,3-bis(hydroxylamino)-2,3-dimethylbutane together with 2,3-diamino-2,3-dimethylbutane and complex Zn salts. A modified procedure was developed for the synthesis of bishydroxylamine, which involves reduction in a Zn/NH(4)Cl/THF-H(2)O system.
    DOI:
    10.1007/bf02496404
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文献信息

  • 1,3,5-TRIAZINE DERIVATIVE, PRODUCTION METHOD THEREOF AND ORGANIC ELECTROLUMINESCENCE DEVICE COMPRISING THIS AS A COMPOSING COMPONENT
    申请人:Yamakawa Tetsu
    公开号:US20090281311A1
    公开(公告)日:2009-11-12
    Since the conventional electron transporters have low thermal stability, the organic electroluminescent devices using them are not sufficient in terms of the compatibility of their luminance and luminous efficiency with device lifetime. A 1,3,5-triazine derivative of formula (1) is obtained by a metal catalyst-aided coupling reaction of a compound of formula (2) with a compound of formula (3), and this is used as a composing component of an organic electroluminescent device. [In the formulae, Ar 1 and Ar 2 represent phenyl group or the like, R 1 and R 2 represent hydrogen atom or the like, R 3 represents methyl or the like, m is an integer of 0 to 2, X represents 2,4-pyridylene or the like, p is 1 or 2, a and b are 1 or 2, a+b is 3, q is 0 or an integer of p or less, M represents —MgR 4 group or the like, R 4 represents chlorine atom or the like, r is p-q, and Y represents a leaving group.]
    由于传统的电子传输体具有低热稳定性,使用它们的有机电致发光器件在亮度和发光效率与器件寿命的兼容性方面不足。通过化合物(2)和化合物(3)的金属催化偶联反应获得式(1)的1,3,5-三嗪衍生物,并将其用作有机电致发光器件的组成部分。[在公式中,Ar1和Ar2代表苯基或类似基团,R1和R2代表氢原子或类似原子团,R3代表甲基或类似基团,m为0至2的整数,X代表2,4-吡啶基或类似基团,p为1或2,a和b为1或2,a+b为3,q为0或小于等于p的整数,M代表-MgR4基团或类似基团,R4代表氯原子或类似原子团,r为p-q,Y代表离去基团。]
  • 1,3,5-TRIAZINE DERIVATIVE, PROCESS FOR PRODUCING SAME, AND ORGANIC ELECTROLUMINESCENT ELEMENT COMPRISING SAME AS CONSTITUENT COMPONENT
    申请人:Aihara Hidenori
    公开号:US20110190494A1
    公开(公告)日:2011-08-04
    A 1,3,5-triazine derivative represented by the formula (1): wherein R 1 , R 2 and R 3 each independently represent a hydrogen atom or a methyl group; X represents a carbon atom or a nitrogen atom; Ar 1 represents a substituted or unsubstituted aromatic hydrocarbon group; Ar 2 represents an C 1-4 alkyl-substituted or unsubstituted aromatic 6-membered heterocyclic group having one or two nitrogen atoms, which may be a condensed ring compound. An organic electroluminescent device comprising the 1,3,5-triazine derivative exhibits low power consumption and long lifetime.
    一种由式(1)表示的1,3,5-三嗪衍生物: 其中R1、R2和R3各自独立地表示氢原子或甲基基团;X表示碳原子或氮原子;Ar1表示取代或未取代的芳香烃基团;Ar2表示具有一个或两个氮原子的取代或未取代的芳香族6元杂环基团,可以是一个缩合环化合物。含有1,3,5-三嗪衍生物的有机电致发光器件具有低功耗和长寿命。
  • PHENYL-SUBSTITUTED 1,3.5-TRIAZINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND ORGANIC ELECTROLUMINESCENT DEVICE CONTAINING THE SAME AS COMPONENT
    申请人:Yamakawa Tetsu
    公开号:US20100249406A1
    公开(公告)日:2010-09-30
    A phenyl-substituted 1,3,5-triazine compound represented by the general formula (1); wherein Ar 1 and Ar 2 independently represent substituted or unsubstituted phenyl, naphthyl or biphenylyl group; R 1 , R 2 and R 3 independently represent hydrogen atom or methyl group; X 1 and X 2 independently represent substituted or unsubstituted phenylene, naphthylene or pyridylene group; p and q independently represent an integer of 0 to 2; and Ar 3 and Ar 4 independently represent substituted or unsubstituted pyridyl or phenyl group. This compound is suitable for an organic electroluminescent device.
    一种代表通式(1)的苯基取代的1,3,5-三嗪化合物; 其中,Ar1和Ar2独立地表示取代或未取代的苯基,萘基或联苯基; R1、R2和R3独立地表示氢原子或甲基基团; X1和X2独立地表示取代或未取代的苯基,萘基或吡啶基; p和q独立地表示0至2的整数; Ar3和Ar4独立地表示取代或未取代的吡啶基或苯基。该化合物适用于有机电致发光器件。
  • PHENYL-SUBSTITUTED 1,3,5-TRIAZINE COMPOUND, PROCESS FOR PRODUCING THE SAME, AND ORGANIC ELECTROLUMINESCENT DEVICE CONTAINING THE SAME AS COMPONENT
    申请人:YAMAKAWA Tetsu
    公开号:US20120313090A1
    公开(公告)日:2012-12-13
    A phenyl-substituted 1,3,5-triazine compound represented by the general formula (1): wherein Ar 1 and Ar 2 independently represent substituted or unsubstituted phenyl, naphthyl or biphenylyl group; R 1 , R 2 and R 3 independently represent hydrogen atom or methyl group; X 1 and X 2 independently represent substituted or unsubstituted phenylene, naphthylene or pyridylene group; p and q independently represent an integer of 0 to 2; and Ar 3 and Ar 4 independently represent substituted or unsubstituted pyridyl or phenyl group. This compound is suitable for an organic electroluminescent device.
    一种含苯基取代的1,3,5-三嗪化合物,其通式表示为(1):其中Ar1和Ar2分别独立地表示取代或未取代的苯基、萘基或联苯基;R1、R2和R3独立地表示氢原子或甲基基团;X1和X2独立地表示取代或未取代的苯基、萘基或吡啶基;p和q独立地表示0至2的整数;Ar3和Ar4独立地表示取代或未取代的吡啶基或苯基。该化合物适用于有机电致发光装置。
  • Cyclic azine derivatives, processes for producing these, and organic electrolumiscent element containing these as component
    申请人:TOSOH CORPORATION
    公开号:EP2818462A1
    公开(公告)日:2014-12-31
    A cyclic azine compound represented by general formula (1): wherein each Ar1 represents a phenyl, naphthyl or pyridyl group, which is unsubstituted or substituted by a C1-4 alkyl group, a phenyl group or a pyridyl group; and A represents a group selected from those which are represented by general formulae (2), (4) and (5), described in the description. The cyclic azine compound is useful for an organic compound layer of fluorescent or phosphorescent EL device.
    由通式(1)代表的环嗪化合物: 其中每个 Ar1 代表苯基、萘基或吡啶基,这些基团未被 C1-4 烷基、苯基或吡啶基取代或被 C1-4 烷基、苯基或吡啶基取代;A 代表选自通式(2)、(4)和(5)的基团。环嗪化合物可用于荧光或磷光 EL 器件的有机化合物层。
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