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N-2,6-dimethylphenylbenzaldehyde imine | 76193-83-4

中文名称
——
中文别名
——
英文名称
N-2,6-dimethylphenylbenzaldehyde imine
英文别名
N-benzylidene-2,6-dimethylamine
N-2,6-dimethylphenylbenzaldehyde imine化学式
CAS
76193-83-4
化学式
C15H15N
mdl
——
分子量
209.291
InChiKey
QEIOUPKHYXBHKA-LFIBNONCSA-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:
    328.0±11.0 °C(Predicted)
  • 密度:
    0.95±0.1 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.05
  • 重原子数:
    16.0
  • 可旋转键数:
    2.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.13
  • 拓扑面积:
    12.36
  • 氢给体数:
    0.0
  • 氢受体数:
    1.0

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:
    参考文献:
    名称:
    Jousseaume Bernard, Vilcot Nathalie, Ricci Alfredo, Tiekink Edward R. T., J. Chem. Soc. Perkin Trans. 1, (1994) N 16, S 2283-2288
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Jousseaume Bernard, Vilcot Nathalie, Ricci Alfredo, Tiekink Edward R. T., J. Chem. Soc. Perkin Trans. 1, (1994) N 16, S 2283-2288
    摘要:
    DOI:
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文献信息

  • Transition metal imide/organic imine metathesis reactions: unexpected observations
    作者:Jacqueline M. McInnes
    DOI:10.1039/a803719a
    日期:——
    Mixtures of [Ti(NBut)Cl2(py)3] 1 and PhC(NAr)H (Ar = C6H3Me2-2,6 or C6H4Me-4) gave quantitative conversion to [Ti(NAr)Cl2(py)3] and PhC(NBut)H, the products of TiNBut/CNAr transition metal imide/organic imine meta-thesis; examination of the kinetics for Ar = C6H4Me-4 showed that the rate limiting step for this process is zero order in [1], demonstrating that these reactions do not involve metal imide particiption in the rate limiting step.
    将[T i(NBut)Cl2(py)3] 1与PhC(NAr)H(Ar = C6H3Me2-2,6或C6H4Me-4)的混合物反应,定量转化为[T i(NAr)Cl2(py)3]和PhC(NBut)H,这些是TiNBut/CNAr过渡亚胺/有机亚胺的元反应产物;对Ar = C6H4Me-4的动力学研究表明,该过程的速率限制步骤在[1]中是零阶,证明这些反应的速率限制步骤不涉及亚胺的参与。
  • CATALYST COMPONENT FOR PROPYLENE POLYMERIZATION, PREPARATION METHOD THEREFOR AND CATALYST HAVING SAME
    申请人:China Petroleum&Chemical Corporation
    公开号:EP3135699A1
    公开(公告)日:2017-03-01
    The present invention discloses a catalyst component for propene polymerization, comprising titanium, magnesium, halogen, and internal electron donor A, wherein said internal electron donor A is selected from the compouns as shown in Formula I, in Formula I, R is selected from hydrogen, hydroxyl, and substituted or unsubstituted C1-C30 hydrocarbyl, preferably from hydrogen, hydroxyl, and substituted or unsubstituted C1-C20 alkyl, C6-C30 aryl, C6-C30 heteroaryl, C7-C30 alkylaryl and C7-C30 arylalkyl; R1 and R2 may be identical to or different from each other, and are selected from hydrogen and substituted or unsubstituted C1-C30 hydrocarbyl, preferably from hydrogen and substituted or unsubstituted C1-C20 alkyl, C6-C30 aryl, C7-C30 alkylaryl and C7-C30 arylalkyl. According to the present invention, by using the compound as shown in Formula I as internal electron donor compound for propene polymerization, the catalyst has a higher activity, and a slow rate of delay of activity. The obtained polymer has not only a wider molecular weight distribution, but also a high melt index and isotacticity.
    本发明公开了一种用于丙烯聚合的催化剂组分,由、卤素和内部电子供体 A 组成,其中所述内部电子供体 A 选自如式 I 所示的化合物、 在式 I 中,R 选自氢、羟基和取代或未取代的 C1-C30 碳氢基,优选选自氢、羟基和取代或未取代的 C1-C20 烷基、C6-C30 芳基、C6-C30 杂芳基、C7-C30 烷芳基和 C7-C30 芳烷基;R1和R2可以彼此相同或不同,并且选自氢和取代或未取代的C1-C30烃基,优选选自氢和取代或未取代的C1-C20烷基、C6-C30芳基、C7-C30烷芳基和C7-C30芳烷基。根据本发明,使用如式 I 所示的化合物作为丙烯聚合的内部电子供体化合物,催化剂具有更高的活性,并且活性延迟的速度较慢。所得到的聚合物不仅分子量分布更广,而且熔融指数和等活度都很高。
  • Catalyst component for propene polymerization, preparation method thereof, and catalyst containing the same
    申请人:China Petroleum & Chemical Corporation
    公开号:US10184017B2
    公开(公告)日:2019-01-22
    The present invention discloses a catalyst component for propene polymerization, comprising titanium, magnesium, halogen, and internal electron donor A, wherein said internal electron donor A is selected from the compounds as shown in Formula I, in Formula I, R is selected from hydrogen, hydroxyl, and substituted or unsubstituted C1-C30 hydrocarbyl, preferably from hydrogen, hydroxyl, and substituted or unsubstituted C1-C20 alkyl, C6-C30 aryl, C6-C30 heteroaryl, C7-C30 alkylaryl and C7-C30 arylalkyl; R1 and R2 may be identical to or different from each other, and are selected from hydrogen and substituted or unsubstituted C1-C30 hydrocarbyl, preferably from hydrogen and substituted or unsubstituted C1-C20 alkyl, C6-C30 aryl, C7-C30 alkylaryl and C7-C30 arylalkyl. According to the present invention, by using the compound as shown in Formula I as internal electron donor compound for propene polymerization, the catalyst has a higher activity, and a slow rate of delay of activity. The obtained polymer has not only a wider molecular weight distribution, but also a high melt index and isotacticity.
    本发明公开了一种用于丙烯聚合的催化剂组分,由、卤素和内部电子供体 A 组成,其中所述内部电子供体 A 选自如式 I 所示的化合物、 在式 I 中,R 选自氢、羟基和取代或未取代的 C1-C30 碳氢基,优选选自氢、羟基和取代或未取代的 C1-C20 烷基、C6-C30 芳基、C6-C30 杂芳基、C7-C30 烷芳基和 C7-C30 芳烷基;R1和R2可以彼此相同或不同,并且选自氢和取代或未取代的C1-C30烃基,优选选自氢和取代或未取代的C1-C20烷基、C6-C30芳基、C7-C30烷芳基和C7-C30芳烷基。根据本发明,使用如式 I 所示的化合物作为丙烯聚合的内部电子供体化合物,催化剂具有更高的活性,并且活性延迟的速度较慢。所得到的聚合物不仅分子量分布更广,而且熔融指数和等活度都很高。
  • A route to sterically crowded benzophenone N-aryl imines
    作者:Lucjan Strekowski、Marek T. Cegla、Donald B. Harden、Suk Bin Kong
    DOI:10.1021/jo00271a047
    日期:1989.5
  • Catalytic synthesis of 1,4-dihydropyridine derivatives using scandium(III) triflate
    作者:Satoshi Kikuchi、Masahiro Iwai、Hiroyuki Murayama、Shin-ichi Fukuzawa
    DOI:10.1016/j.tetlet.2007.11.003
    日期:2008.1
    Scandium(III) triflate smoothly catalyzed the reaction of imines with ethyl propiolate (2.5 equiv) to produce the corresponding N-substituted 1,4-dihydropyridines in good yields in toluene or BTF under reflux conditions. It also catalyzed the reaction of aniline and ethyl propiolate (3.2 equiv) to give another 1,4-dihydropyridine bearing three ester groups in moderate yield under the same conditions. (c) 2007 Elsevier Ltd. All rights reserved.
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