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苯基丙酮酸缩氨基脲 | 81118-82-3

中文名称
苯基丙酮酸缩氨基脲
中文别名
——
英文名称
phenyl pyruvic acid semicarbazone
英文别名
Phenylbrenztraubensaeuresemicarbazon;Phenylpyruvic acid semicarbazone;2-(carbamoylhydrazinylidene)-3-phenylpropanoic acid
苯基丙酮酸缩氨基脲化学式
CAS
81118-82-3
化学式
C10H11N3O3
mdl
——
分子量
221.216
InChiKey
YJGYBVXMGQWGRT-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
  • 重原子数:
    16
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    105
  • 氢给体数:
    3
  • 氢受体数:
    4

反应信息

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文献信息

  • Manganese(II) and copper(II) complexes of some nitrogenoxygen and nitrogensulphur donor ligands
    作者:S. Chandra、K.K. Sharma
    DOI:10.1016/s0277-5387(00)84657-4
    日期:1984.1
    Abstract Manganese(II) and copper(II) complexes of the type M(ligandH)2 with some nitrogenoxygen and nitrogensulphur donor ligands (HL) viz. phenylpyruvic acid semicarbazone (ppysc), 4-methylphenylpyruvic acid semicarbazone (4-mppysc), phenylpyruvic acid thiosemicarbazone (ppytsc) and 4-methylphenyl pyruvic acid thiosemicarbazone (4-ppytsc), have been synthesised. All the complexes have been characterised
    摘要M(配体H)2型(II)和(II)配合物具有一些氮氧和氮供体配体(HL)。已经合成了苯基丙酮酸半卡巴zone(ppysc),4-甲基苯基丙酮酸半卡巴zone(4-mppysc),苯基丙酮代半碳酰胺(ppytsc)和4-甲基苯基丙酮代半碳zone(4-ppytsc)。所有配合物的特征都在于磁矩测量,红外电子和电子自旋共振的特殊研究。所有的配体表现为三齿的。
  • Synthesis of Some 5-Alkyl-6-azauracils<sup>1</sup>
    作者:PAULINE K. CHANG
    DOI:10.1021/jo01106a038
    日期:1958.12
  • Synthesis and antimicrobial evaluation of 6-azauracil non-nucleosides
    作者:Nasser R. El-Brollosy
    DOI:10.1007/s00706-008-0948-7
    日期:2008.12
    The present study describes synthesis and antimicrobial evaluation of a series of novel 6-azauracil non-nucleosides. Reaction of silylated 6-azauracils with the appropriate chloroethers gave the corresponding non-nucleosides. 1-(Allyloxymethy)6-azauracils and non-nucleosides bearing indanyl, cyclohexenyl, and cyclohexyl moieties were obtained via silylation of 6-azauracils followed by treatment with the appropriate acetals. Selected compounds were tested for their in vitro antimicrobial activity against a panel of standard strains of Gram-positive and Gram-negative bacteria and the yeast-like pathogenic fungus Candida albicans. Four compounds showed marked inhibitory activity particularly against the tested Gram-positive bacteria.
  • Synthetic and Antiviral Studies on Certain Acyclic Nucleosides of 5-Benzyl-6-Azauracil Derivatives
    作者:Yeh-Long Chen、Shwu-Jing Chen、Kuan-Han Lee、Bor-Ruey Huang、Cherng-Chyi Tzeng
    DOI:10.1080/07328319308018563
    日期:1993.11
    Several 5-(4-substituted benzyl)-6-azauracils have been synthesized from the corresponding benzaldehydes. The 5-benzyl-6-azauracils were silylated with hexamethyldisilazane and then glycosylated with aliphatic halides, e.g., (2-acetoxyethoxy)methyl bromide and 1,3-dibenzyloxy-2-chloromethoxypropane, to give protected acyclic nucleosides which were deprotected to afford acyclonucleosides of 5-(4-substituted benzyl)-6-azauracils. None of the compounds exhibited significant antiviral activity against herpes simplex virus type 1 (HSV-1) and type 2 (HSV-2) in vitro.
  • Stoermer; Kirchner, Chemische Berichte, 1920, vol. 53, p. 1299
    作者:Stoermer、Kirchner
    DOI:——
    日期:——
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