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(E)-N-(2,6-dimethylphenyl)formamidine

中文名称
——
中文别名
——
英文名称
(E)-N-(2,6-dimethylphenyl)formamidine
英文别名
N'-(2,6-dimethylphenyl)methanimidamide
(E)-N-(2,6-dimethylphenyl)formamidine化学式
CAS
——
化学式
C9H12N2
mdl
——
分子量
148.208
InChiKey
HGLSGOCZYXRXNN-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):
    1.7
  • 重原子数:
    11
  • 可旋转键数:
    1
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.22
  • 拓扑面积:
    38.4
  • 氢给体数:
    1
  • 氢受体数:
    1

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

反应信息

  • 作为反应物:
    描述:
    (E)-N-(2,6-dimethylphenyl)formamidine正丁基锂 作用下, 以 四氢呋喃乙醚正戊烷 为溶剂, 反应 16.0h, 生成 [(E)-N'-(2,6-dimethylphenyl)-N-(diisopropylphosphino)formamidine](THF)CrCl3
    参考文献:
    名称:
    [EN] PHOSPHINYL FORMAMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS
    [FR] COMPOSÉS PHOSPHINYL FORMAMIDINE, COMPLEXES MÉTALLIQUES, SYSTÈMES DE CATALYSEUR, ET LEUR UTILISATION POUR OLIGOMÉRISER OU POLYMÉRISER DES OLÉFINES
    摘要:
    描述了N2-磷酰基甲酰胺化合物和N2-磷酰基甲酰胺金属盐配合物。还公开了制备N2-磷酰基甲酰胺化合物和N2-磷酰基甲酰胺金属盐配合物的方法。还公开了利用N2-磷酰基甲酰胺金属盐配合物的催化剂体系,以及利用N2-磷酰基胺化合物和N2-磷酰基胺金属盐配合物进行烯烃的寡聚和/或聚合的用途。
    公开号:
    WO2015094207A1
  • 作为产物:
    描述:
    2,6-二甲基苯胺碳酸氢铵对甲苯磺酸 作用下, 以 甲醇 为溶剂, 反应 24.0h, 生成 (E)-N-(2,6-dimethylphenyl)formamidine
    参考文献:
    名称:
    [EN] PHOSPHINYL FORMAMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS
    [FR] COMPOSÉS PHOSPHINYL FORMAMIDINE, COMPLEXES MÉTALLIQUES, SYSTÈMES DE CATALYSEUR, ET LEUR UTILISATION POUR OLIGOMÉRISER OU POLYMÉRISER DES OLÉFINES
    摘要:
    描述了N2-磷酰基甲酰胺化合物和N2-磷酰基甲酰胺金属盐配合物。还公开了制备N2-磷酰基甲酰胺化合物和N2-磷酰基甲酰胺金属盐配合物的方法。还公开了利用N2-磷酰基甲酰胺金属盐配合物的催化剂体系,以及利用N2-磷酰基胺化合物和N2-磷酰基胺金属盐配合物进行烯烃的寡聚和/或聚合的用途。
    公开号:
    WO2015094207A1
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文献信息

  • HDAC INHIBITORS AND THERAPEUTIC METHODS USING THE SAME
    申请人:Kozikowski Alan
    公开号:US20140128408A1
    公开(公告)日:2014-05-08
    Histone deacetylases inhibitors (HDACIs) and compositions containing the same are disclosed. Methods of treating diseases and conditions wherein inhibition of HDAC provides a benefit, like a cancer, a neurodegenerative disorder, a peripheral neuropathy, a neurological disease, traumatic brain injury, stroke, hypertension, malaria, an autoimmune disease, autism, autism spectrum disorders, and inflammation, also are disclosed.
    本发明公开了组蛋白去乙酰化酶抑制剂(HDACIs)及其组成物。公开了治疗疾病和状况的方法,其中抑制HDAC提供了益处,如癌症、神经退行性疾病、周围神经病变、神经疾病、创伤性脑损伤、中风、高血压、疟疾、自身免疫疾病、自闭症、自闭症谱系障碍和炎症。
  • Multinuclear Copper(I) and Silver(I) Amidinate Complexes: Synthesis, Luminescence, and CS<sub>2</sub> Insertion Reactivity
    作者:Andrew C. Lane、Matthew V. Vollmer、Charles H. Laber、Doris Y. Melgarejo、Gina M. Chiarella、John P. Fackler、Xinzheng Yang、Gary A. Baker、Justin R. Walensky
    DOI:10.1021/ic501694d
    日期:2014.11.3
    Dinuclear Cu(I) and Ag(I) complexes, Cu-2[(2,6-Me2C6H3N)(2)C(H)](2), 1, Ag2[(2,6-Me2C6H3N)(2)C(H)](2), 2, Cu-2[2,6-(i)Pr2C6H3N)(2)C(H)](2), 3, and Ag-2[(2,6-(i)Pr2C6H3N)(2)C(H)](2), 4, were synthesized from reactions of [Cu(NCCH3)4][PF6] with Na[(2,6-R2C6H3N)2C(H)] and AgO2CCH3 with [Et3NH][(2,6-R2C6H3N2C(H)], R = Me, (i)Pr. Carbon disulfide was observed to insert into the metal-nitrogen bonds of 1 to produce Cu-4[CS2(2,6-Me2C6H3NC(H)-NC6H3Me2)]4, 5, with a Cu4S8 core, which represents a rare transformation of dinuclear to tetranuclear species. Insertion is also observed with 2 and CS2, with the product likely being polymeric, 6. With the (i)Pr-derivatives, CS2 insertion was also observed, albeit at much slower rate, with 3 and 4 producing hexanuclear clusters, M-6[CS2(2,6-Me2C6H3NC(H)-NC6H3Me2)](6), M = Cu, 7; Ag, 8. Complexes 1 and 5 display green luminescence, a feature not shared by their Ag(I) analogs nor with 3. Notably, oxygen acts as a collisional quencher of the luminescence from 1 and 5 at a rate faster than most metal-based quenchometric O-2 sensors. For example, we find that complex 1 can be rapidly and reversibly quenched by oxygen, presenting a nearly 6-fold drop in intensity upon switching from nitrogen to an aerated atmosphere. The results here provide a platform from which further group 11 amidinate reactivity can be explored.
  • PHOSPHINYL FORMAMIDINE COMPOUNDS, METAL COMPLEXES, CATALYST SYSTEMS, AND THEIR USE TO OLIGOMERIZE OR POLYMERIZE OLEFINS
    申请人:Chevron Phillips Chemical Company LP
    公开号:EP3083646A1
    公开(公告)日:2016-10-26
  • Phosphinyl Formamidine Compounds, Metal Complexes, Catalyst Systems, and Their Use to Oligomerize or Polymerize Olefins
    申请人:Chevron Phillips Chemical Company LP
    公开号:US20160375431A1
    公开(公告)日:2016-12-29
    N 2 -phosphinyl formamidine compounds and N 2 -phosphinyl formamidine metal salt complexes are described. Methods for making N 2 -phosphinyl formamidine compounds and N 2 -phosphinyl formamidine metal salt complexes are also disclosed. Catalyst systems utilizing the N 2 -phosphinyl formamidine metal salt complexes are also disclosed along with the use of the N 2 -phosphinyl amidine compounds and N 2 -phosphinyl amidinate metal salt complexes for the oligomerization and/or polymerization of olefins.
  • US9962689B2
    申请人:——
    公开号:US9962689B2
    公开(公告)日:2018-05-08
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