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5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole | 159053-03-9

中文名称
——
中文别名
——
英文名称
5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole
英文别名
2-(3-phenyl-1H-1,2,4-triazol-5-yl)pyrazine
5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole化学式
CAS
159053-03-9
化学式
C12H9N5
mdl
MFCD11557411
分子量
223.237
InChiKey
YTWJCQLAVXEMMS-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:
    485.9±55.0 °C(Predicted)
  • 密度:
    1.303±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    67.4
  • 氢给体数:
    1
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole氢氧化钾苄基三乙基氯化铵sodium methylate 作用下, 以 甲醇二氯甲烷 为溶剂, 反应 30.0h, 生成 1-(β-1-D-glucopyranosyl)-5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole
    参考文献:
    名称:
    Synthesis and antiviral activity of some new 1H-1,2,4-triazole derivatives
    摘要:
    A series of new 1H-1,2,4-triazole derivatives was synthesised and evaluated in vitro for activity against various DNA and RNA viruses. Compounds 1-benzyl-5-(4-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 2b, 1-benzyl-5-(3-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 2c and 1-[(2-hydroxyethoxy)methyl]-5-(3-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 4h proved active against reovirus-1, and compounds 1-[(2-hydroxyethoxy)methyl]-5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole 4f and 1-[(2-hydroxyethoxy)methyl]-5-(3-methylphenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole 4h against parainfluenza-3 virus, in Vero cells at concentrations that were 5- to 40-fold lower than the cytotoxic concentrations required to alter normal cell morphology.
    DOI:
    10.1016/0223-5234(94)90152-x
  • 作为产物:
    描述:
    吡嗪-2-甲酰肼苯甲亚胺酸乙酯 反应 5.0h, 以87%的产率得到5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole
    参考文献:
    名称:
    Synthesis and antiviral activity of some new 1H-1,2,4-triazole derivatives
    摘要:
    A series of new 1H-1,2,4-triazole derivatives was synthesised and evaluated in vitro for activity against various DNA and RNA viruses. Compounds 1-benzyl-5-(4-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 2b, 1-benzyl-5-(3-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 2c and 1-[(2-hydroxyethoxy)methyl]-5-(3-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 4h proved active against reovirus-1, and compounds 1-[(2-hydroxyethoxy)methyl]-5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole 4f and 1-[(2-hydroxyethoxy)methyl]-5-(3-methylphenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole 4h against parainfluenza-3 virus, in Vero cells at concentrations that were 5- to 40-fold lower than the cytotoxic concentrations required to alter normal cell morphology.
    DOI:
    10.1016/0223-5234(94)90152-x
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文献信息

  • Structural and photophysical characterisation of coordination and optical isomers of mononuclear ruthenium(ii) polypyridyl 1,2,4-triazole complexesElectronic supplementary information (ESI) available: analytical and semipreparative HPLC chromatograms, CD and UV/vis spectra. See http://www.rsc.org/suppdata/dt/b3/b301961f/
    作者:Wesley R. Browne、Dusan Hesek、John F. Gallagher、Christine M. O'Connor、J. Scott Killeen、Fumiko Aoki、Hitoshi Ishida、Yoshihisa Inoue、Claudio Villani、Johannes G. Vos
    DOI:10.1039/b301961f
    日期:——
    The X-ray crystal structure of the N2 isomers of the Ru(bipy)2 complexes of Hphpztr (1) and Hpztr (2), (bipy = 2,2′-bipyridine, Hphpztr = 2-(5′-phenyl-4′H-[1,2,4]triazol-3′-yl)pyrazine and Hpztr = 2-(4′H-[1,2,4]triazol-3′-yl)pyrazine) are reported. The molecular structure obtained for 2 demonstrates an interesting structural aspect in the sharing of a single proton between two molecular units. The isolation of the Δ and Λ stereoisomers of 1 and [Ru(phen)2(pztr)]+ (phen = 1,10-phenanthroline) (3) by semipreparative HPLC is also reported. The compounds obtained are characterised by electronic spectroscopy and particular attention is paid to the photophysical properties of Δ and Λ isomers of 1 and 3, in chiral enantiopure and racemic solvents.
    报告了Hphpztr(1)和Hpztr(2)的Ru(bipy)2复合物N2异构体的X射线晶体结构(bipy = 2,2′-联吡啶,Hphpztr = 2-(5′-苯基-4′H-[1,2,4]三唑-3′-基)吡嗪,Hpztr = 2-(4′H-[1,2,4]三唑-3′-基)吡嗪)。2的分子结构表明,两个分子单元之间共享一个质子,这是一个有趣的结构方面。还报告了通过半制备HPLC分离1和[Ru(phen)2(pztr)]+的Δ和Λ立体异构体(phen = 1,10-菲咯啉)的分离(3)。所获得的化合物的特征在于电子光谱,并特别关注1和3的Δ和Λ异构体在手性对映纯溶剂和消旋溶剂中的光物理性质。
  • Resin composition
    申请人:KONICA MINOLTA, INC.
    公开号:US10012777B2
    公开(公告)日:2018-07-03
    The present invention provides a resin composition capable of forming a film exhibiting a small humidity-dependent variation in optical values; a triazole compound to be incorporated into the resin composition; an optical film and an optical lens, each of which is prepared from the resin composition and exhibits a small humidity-dependent variation in optical values; and a polarizing plate, a circularly polarizing plate, and an image display device, each of which includes the optical film and exhibits excellent moisture resistance. The resin composition of the present invention contains a resin and a compound having a 5-membered or 6-membered aromatic hydrocarbon or heterocyclic ring, wherein the resin is a hygroscopic resin, the compound has at least three specific aromatic rings having a specific NICS value, and the specific aromatic rings are bonded to one another via a single bond or one or two atoms.
    本发明提供了一种能够形成薄膜的树脂组合物,其光学值随湿度的变化很小;一种三唑化合物,可掺入该树脂组合物中;一种光学薄膜和一种光学透镜,它们分别由该树脂组合物制备而成,其光学值随湿度的变化很小;以及一种偏光板、一种圆偏光板和一种图像显示装置,它们分别包括该光学薄膜,并具有优异的防潮性能。本发明的树脂组合物包含一种树脂和一种具有 5 元或 6 元芳香烃环或杂环的化合物,其中树脂是一种吸湿性树脂,化合物具有至少三个具有特定 NICS 值的特定芳香环,特定芳香环通过单键或一个或两个原子相互结合。
  • RESIN COMPOSITION, TRIAZOLE COMPOUND, OPTICAL FILM, POLARIZING PLATE, OPTICAL LENS, CIRCULARLY POLARIZING PLATE AND IMAGE DISPLAY DEVICE
    申请人:KONICA MINOLTA, INC.
    公开号:US20150338563A1
    公开(公告)日:2015-11-26
    The present invention provides a resin composition capable of forming a film exhibiting a small humidity-dependent variation in optical values; a triazole compound to be incorporated into the resin composition; an optical film and an optical lens, each of which is prepared from the resin composition and exhibits a small humidity-dependent variation in optical values; and a polarizing plate, a circularly polarizing plate, and an image display device, each of which includes the optical film and exhibits excellent moisture resistance. The resin composition of the present invention contains a resin and a compound having a 5-membered or 6-membered aromatic hydrocarbon or heterocyclic ring, wherein the resin is a hygroscopic resin, the compound has at least three specific aromatic rings having a specific NICS value, and the specific aromatic rings are bonded to one another via a single bond or one or two atoms.
  • TRIAZOLE COMPOUND
    申请人:KONICA MINOLTA, INC.
    公开号:US20180203175A1
    公开(公告)日:2018-07-19
    A triazole compound having a structure represented by the following Formula (1.2): wherein Z represents a structure represented by the following Formula (1.2a), q is 2 or 3, and at least two structures Z bonded to the benzene ring of Formula (1.2) and are located in the ortho- or meta-position relative to each other: wherein R 10 represents a hydrogen atom, an alkyl group, or an alkoxy group, p represents an integer of 1 to 5, and * represents a position at which the structure is bonded to the benzene ring.
  • Synthesis and antiviral activity of some new 1H-1,2,4-triazole derivatives
    作者:OG Todoulou、AE Papadaki-Valiraki、S Ikeda、E De Clercq
    DOI:10.1016/0223-5234(94)90152-x
    日期:1994.1
    A series of new 1H-1,2,4-triazole derivatives was synthesised and evaluated in vitro for activity against various DNA and RNA viruses. Compounds 1-benzyl-5-(4-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 2b, 1-benzyl-5-(3-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 2c and 1-[(2-hydroxyethoxy)methyl]-5-(3-methylphenyl)-3-(2-pyrazinyl)-1H-1,2,4-triazole 4h proved active against reovirus-1, and compounds 1-[(2-hydroxyethoxy)methyl]-5-phenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole 4f and 1-[(2-hydroxyethoxy)methyl]-5-(3-methylphenyl-3-(2-pyrazinyl)-1H-1,2,4-triazole 4h against parainfluenza-3 virus, in Vero cells at concentrations that were 5- to 40-fold lower than the cytotoxic concentrations required to alter normal cell morphology.
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