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4-Pyridincarboxaldehyd-2-benzothiazolylhydrazon | 51287-67-3

中文名称
——
中文别名
——
英文名称
4-Pyridincarboxaldehyd-2-benzothiazolylhydrazon
英文别名
N-(pyridin-4-ylmethylideneamino)-1,3-benzothiazol-2-amine
4-Pyridincarboxaldehyd-2-benzothiazolylhydrazon化学式
CAS
51287-67-3
化学式
C13H10N4S
mdl
MFCD00435835
分子量
254.315
InChiKey
JLIFGFRXBLCQSK-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

  • 熔点:
    224 °C(Solv: ethanol (64-17-5))
  • 沸点:
    441.5±37.0 °C(Predicted)
  • 密度:
    1.34±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    18
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    78.4
  • 氢给体数:
    1
  • 氢受体数:
    5

SDS

SDS:dcd5bb99575077f600e13359f41b9971
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反应信息

  • 作为反应物:
    描述:
    4-Pyridincarboxaldehyd-2-benzothiazolylhydrazon2,2-(乙烯二硫代)二苯胺盐酸 、 sodium nitrite 作用下, 以 异丙醇 为溶剂, 反应 0.33h, 生成
    参考文献:
    名称:
    Catalytic activity of new nickel(II) formazanates in ethylene oligomerization
    摘要:
    Thirteen mono- and three bisformazans containing one system of azahydrazone bonds have been synthesized, as well as mono- and binuclear complexes on their basis. The kinetic features of ethylene oligomerization in the presence of catalytic systems on the basis of AlEtCl2-activated Ni(II) formazanates differing in composition and structure have been studied. The structures of the mono- and binuclear complexes differ by substituents in the formazan ligand, which have an effect on the activity of the systems and the product composition. The catalytic activity of the binuclear complexes is several times below that of mononuclear Ni(II) formazanates.
    DOI:
    10.1134/s0965544112010124
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文献信息

  • Catalytic activity of new nickel(II) formazanates in ethylene oligomerization
    作者:A. V. Zaidman、I. I. Khasbiullin、G. P. Belov、I. G. Pervova、I. N. Lipunov
    DOI:10.1134/s0965544112010124
    日期:2012.1
    Thirteen mono- and three bisformazans containing one system of azahydrazone bonds have been synthesized, as well as mono- and binuclear complexes on their basis. The kinetic features of ethylene oligomerization in the presence of catalytic systems on the basis of AlEtCl2-activated Ni(II) formazanates differing in composition and structure have been studied. The structures of the mono- and binuclear complexes differ by substituents in the formazan ligand, which have an effect on the activity of the systems and the product composition. The catalytic activity of the binuclear complexes is several times below that of mononuclear Ni(II) formazanates.
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同类化合物

(1Z)-1-(3-乙基-5-羟基-2(3H)-苯并噻唑基)-2-丙酮 齐拉西酮砜 阳离子蓝NBLH 阳离子荧光黄4GL 锂2-(4-氨基苯基)-5-甲基-1,3-苯并噻唑-7-磺酸酯 铜酸盐(4-),[2-[2-[[2-[3-[[4-氯-6-[乙基[4-[[2-(硫代氧代)乙基]磺酰]苯基]氨基]-1,3,5-三嗪-2-基]氨基]-2-(羟基-kO)-5-硫代苯基]二氮烯基-kN2]苯基甲基]二氮烯基-kN1]-4-硫代苯酸根(6-)-kO]-,(1:4)氢,(SP-4-3)- 铜羟基氟化物 钾2-(4-氨基苯基)-5-甲基-1,3-苯并噻唑-7-磺酸酯 钠3-(2-{(Z)-[3-(3-磺酸丙基)-1,3-苯并噻唑-2(3H)-亚基]甲基}[1]苯并噻吩并[2,3-d][1,3]噻唑-3-鎓-3-基)-1-丙烷磺酸酯 邻氯苯骈噻唑酮 西贝奈迪 螺[3H-1,3-苯并噻唑-2,1'-环戊烷] 螺[3H-1,3-苯并噻唑-2,1'-环己烷] 葡萄属英A 草酸;N-[1-[4-(2-苯基乙基)哌嗪-1-基]丙-2-基]-2-丙-2-基氧基-1,3-苯并噻唑-6-胺 苯酰胺,N-2-苯并噻唑基-4-(苯基甲氧基)- 苯酚,3-[[2-(三苯代甲基)-2H-四唑-5-基]甲基]- 苯胺,N-(3-苯基-2(3H)-苯并噻唑亚基)- 苯碳杂氧杂脒,N-1,2-苯并异噻唑-3-基- 苯甲基2-甲基哌啶-1,2-二羧酸酯 苯并噻唑正离子,2-[3-(1,3-二氢-1,3,3-三甲基-2H-吲哚-2-亚基)-1-丙烯-1-基]-3-乙基-,碘化(1:1) 苯并噻唑正离子,2-[(2-乙氧基-2-羰基乙基)硫代]-3-甲基-,溴化 苯并噻唑啉 苯并噻唑-d4 苯并噻唑-6-腈 苯并噻唑-5-羧酸 苯并噻唑-5-硼酸频哪醇酯 苯并噻唑-4-醛 苯并噻唑-4-乙酸 苯并噻唑-2-磺酸钠 苯并噻唑-2-磺酸 苯并噻唑-2-磺酰氟 苯并噻唑-2-甲醛 苯并噻唑-2-甲酸 苯并噻唑-2-甲基甲胺 苯并噻唑-2-基磺酰氯 苯并噻唑-2-基叠氮化物 苯并噻唑-2-基-邻甲苯-胺 苯并噻唑-2-基-己基-胺 苯并噻唑-2-基-(4-氯-苯基)-胺 苯并噻唑-2-基-(4-氟-苯基)-胺 苯并噻唑-2-基-(4-乙氧基-苯基)-胺 苯并噻唑-2-基-(2-甲氧基-苯基)-胺 苯并噻唑-2-基-(2,6-二甲基-苯基)-胺 苯并噻唑-2-基(对甲苯基)甲醇 苯并噻唑-2-乙酸甲酯 苯并噻唑-2-乙腈 苯并噻唑-2(3H)-酮N2-[1-(吡啶-4-基)乙亚基]腙 苯并噻唑-2 - 丙基 苯并噻唑,6-(3-乙基-2-三氮烯基)-2-甲基-(8CI)