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2-(2,6-二甲基苯基硫代)苯胺 | 33264-60-7

中文名称
2-(2,6-二甲基苯基硫代)苯胺
中文别名
——
英文名称
2-(2,6-dimethylphenylthio)benzenamine
英文别名
2,6-Dimethylphenyl-2-aminophenylsulfid;2-Aminophenyl-2,6-dimethylphenylsulfid;2-(2,6-Dimethylphenyl)sulfanylaniline
2-(2,6-二甲基苯基硫代)苯胺化学式
CAS
33264-60-7
化学式
C14H15NS
mdl
——
分子量
229.346
InChiKey
AWCMNPKTLMOABD-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:
    315.8±30.0 °C(Predicted)
  • 密度:
    1.14±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.14
  • 拓扑面积:
    51.3
  • 氢给体数:
    1
  • 氢受体数:
    2

安全信息

  • 海关编码:
    2930909090

SDS

SDS:ee8a91c55fe2b7245c7db5c514308d13
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反应信息

  • 作为反应物:
    描述:
    2-(2,6-二甲基苯基硫代)苯胺1-苯基-1,3-丁二酮溶剂黄146 作用下, 以 乙醇 为溶剂, 反应 24.0h, 以72%的产率得到3-{2-[(2,6-Dimethylphenyl)sulfanyl]anilino}-1-phenylbut-2-en-1-one
    参考文献:
    名称:
    Organic compounds containing heteroatoms and their use in ziegler-natta catalyst with single activation center
    摘要:
    公开号:
    EP2039677B1
  • 作为产物:
    描述:
    2-(2-azido-phenylsulfanyl)-1,3-dimethyl-benzene 以 萘烷 为溶剂, 生成 2-(2,6-二甲基苯基硫代)苯胺
    参考文献:
    名称:
    用三价磷试剂还原亚硝基化合物。第九部分 2,6-二取代的芳基2-硝基苯基和2,6-二取代的芳基2-叠氮基苯基硫化物反应中的“受阻邻”效应:一系列新的腈诱导的芳族重排
    摘要:
    鉴于有证据表明,将芳基2-硝基苯基硫化物与亚磷酸三乙酯脱氧并进行相应的2-叠氮基衍生物的热解是通过重排进行的,该重排涉及芳基中的游离邻位,从而产生吩噻嗪,相应的反应涉及硝基化合物和已经完成了两个邻位都被阻断的叠氮化物。这些导致了一系列新的芳族重排,其中2-硝基苯基2,6-二甲基-,2,6-二甲氧基-,2,6-二氯-,2-氯-6-甲基-,2,4,6-三甲基和2,6-二乙氧基羰基苯基硫化物以及(除了姓氏例外)相应的2-叠氮基衍生物分别转化为5,11-二氢-4-甲基二苯并[ b,e] [1,4] thiazepine(17),1-和1,2-二甲氧基吩噻嗪(通过新型的脱甲氧基作用和1,4-甲氧基基团转移),1-和4-氯吩噻嗪,1-和4-甲基吩噻嗪, 5,11-二氢-2,4-二甲基二苯并[ b,e ] [1,4]噻嗪(23)和4a H-吩噻嗪-1,4a-二羧酸二乙酯(50)。在两种氯取代的衍生物的情
    DOI:
    10.1039/j39710002621
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文献信息

  • Synthesis, Characterization, and Highly Selective Ethylene Dimerization to 1-Butene of [O−NX]Ni(II) Complexes
    作者:Chongjie Xu、Qi Shen、Xiuli Sun、Yong Tang
    DOI:10.1002/cjoc.201100443
    日期:2012.5
    series of nickel(II) complexes have been synthesized and characterized. Molecular structure analysis exhibits that a square planar geometry around nickel is adopted. Upon activation with MAO, these nickel(II) complexes are efficient in catalyzing the ethylene dimerization, providing 1‐butene with an activity of up to 1.4×107 g/(mol·h·atm). The heteroatoms of the sidearm in the complexes were proved to
    已经合成和表征了一系列镍(II)配合物。分子结构分析表明,采用了围绕镍的正方形平面几何形状。通过MAO活化后,这些镍(II)络合物可有效催化乙烯二聚,从而提供1-丁烯,其活性最高可达1.4×10 7 g /(mol·h·atm)。络合物中侧臂的杂原子被证明对1-丁烯的活性和选择性有很大的影响。
  • ORGANIC COMPOUNDS CONTAINING HETEROATOMS AND THEIR USE IN ZIEGLER-NATTA CATALYST WITH SINGLE ACTIVATION CENTER
    申请人:SHANGHAI INSTITUTE OF ORGANIC CHEMISTRY, CHINESE ACADEMY OF SCIENCES
    公开号:EP2039677A1
    公开(公告)日:2009-03-25
    Organic compounds containing heteroatoms and their use in preparing Ziegler-Natta (Z-N) catalyst with single activation center. The Z-N olefin polymerization catalyst is prepared by adding organic or inorganic solid carrier or compound of them which is pre-activated by heating or pre-treated chemically, organic compound containing heteroatoms and metallic compound into magnesium compound/tetrahydrofuran solution. The Z-N olefin polymerization catalyst prepared in the present invention is fluidizable powder and can prepare ethene homopolymer and copolymer of controllable construction with high catalytic activity, during homo-polymerization and combined polymerization with alpha-olefin of C3-C8 under action of catalyst promoter such as alkyl aluminium, alkyl aluminoxane, and so on.
    含有杂原子的有机化合物及其在制备具有单活化中心的齐格勒-纳塔(Z-N)催化剂中的应用。Z-N 烯烃聚合催化剂的制备方法是在镁化合物/四氢呋喃溶液中加入经加热预活化或化学预处理的有机或无机固体载体或它们的化合物、含杂原子的有机化合物和金属化合物。本发明制备的 Z-N 烯烃聚合催化剂为可流动粉末,在烷基铝、烷基铝氧烷等催化剂促进剂的作用下,与 C3-C8 α-烯烃进行均聚和联合聚合时,可制备结构可控、催化活性高的乙烯均聚物和共聚物。
  • CADOGAN J. I. G.; TWEDDLE N. J., J. CHEM. SOC. PERKIN TRANS., PART 1, 1979, NO 5, 1278-1284
    作者:CADOGAN J. I. G.、 TWEDDLE N. J.
    DOI:——
    日期:——
  • CLASS OF ORGANIC COMPOUNDS CONTAINING HETEROATOM AND ITS APPLICATIONS IN PREPARING SINGLE-SITE ZIEGLER-NATTA CATALYST
    申请人:TANG Yong
    公开号:US20090137383A1
    公开(公告)日:2009-05-28
    Organic compounds containing heteroatoms and their use in preparing Ziegler-Natta (Ziegler-Natta) catalyst with single activation center. The Ziegler-Natta olefin polymerization catalyst is preparing by adding organic or inorganic solid carrier or compound of them which is pre-activated by heating or pre-treated chemically, organic compound containing heteroatoms and metallic compound into magnesium compound/tetrahydrofuran solution. The Ziegler-Natta olefin polymerization catalyst prepared in the present invention is fluidizable powder and can prepare ethene homopolymer and copolymer of controllable construction with high catalytic activity, during homo-polymerization and combined polymerization with alpha-olefin of C 3 ˜C 18 under action of catalyst promoter such as alkyl aluminum, alkyl aluminoxane, and so on.
  • Reduction of nitro- and nitroso-compounds by tervalent phosphorus reagents. Part IX. The ‘blocked ortho’ effect in reactions of 2,6-di-substituted aryl 2-nitrophenyl and 2,6-disubstituted aryl 2-azidophenyl sulphides: a new series of nitrene-induced aromatic rearrangements
    作者:J. I. G. Cadogan、S. Kulik
    DOI:10.1039/j39710002621
    日期:——
    thermolysis of the corresponding 2-azido-derivatives proceed via rearrangement involving a free ortho-position in the aryl group to give phenothiazines, corresponding reactions involving nitro-compounds and azides in which both ortho-positions are blocked have been carried out. These have led to a new series of aromatic rearrangements whereby 2-nitrophenyl 2,6-dimethyl-, 2,6-dimethoxy-, 2,6-dichloro-
    鉴于有证据表明,将芳基2-硝基苯基硫化物与亚磷酸三乙酯脱氧并进行相应的2-叠氮基衍生物的热解是通过重排进行的,该重排涉及芳基中的游离邻位,从而产生吩噻嗪,相应的反应涉及硝基化合物和已经完成了两个邻位都被阻断的叠氮化物。这些导致了一系列新的芳族重排,其中2-硝基苯基2,6-二甲基-,2,6-二甲氧基-,2,6-二氯-,2-氯-6-甲基-,2,4,6-三甲基和2,6-二乙氧基羰基苯基硫化物以及(除了姓氏例外)相应的2-叠氮基衍生物分别转化为5,11-二氢-4-甲基二苯并[ b,e] [1,4] thiazepine(17),1-和1,2-二甲氧基吩噻嗪(通过新型的脱甲氧基作用和1,4-甲氧基基团转移),1-和4-氯吩噻嗪,1-和4-甲基吩噻嗪, 5,11-二氢-2,4-二甲基二苯并[ b,e ] [1,4]噻嗪(23)和4a H-吩噻嗪-1,4a-二羧酸二乙酯(50)。在两种氯取代的衍生物的情
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