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1-phenyl-5-(4-chlorophenyl)-1H-tetrazole | 99137-13-0

中文名称
——
中文别名
——
英文名称
1-phenyl-5-(4-chlorophenyl)-1H-tetrazole
英文别名
5-(4-chlorophenyl)-1-phenyl-1H-tetrazole;5-(4-chlorophenyl)-1-phenyltetrazole;5-(4-chloro-phenyl)-1-phenyl-1H-tetrazole;5-(4-Chlor-phenyl)-1-phenyl-1H-tetrazol
1-phenyl-5-(4-chlorophenyl)-1H-tetrazole化学式
CAS
99137-13-0
化学式
C13H9ClN4
mdl
——
分子量
256.694
InChiKey
ONSPRELSXLHYSI-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):
    3.5
  • 重原子数:
    18
  • 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:
    43.6
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

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文献信息

  • Transition-metal-free multinitrogenation of amides by C–C bond cleavage: a new approach to tetrazoles
    作者:Lian-Hua Li、Zhi-Jie Niu、Ying-Xiu Li、Yong-Min Liang
    DOI:10.1039/c8cc06324a
    日期:——
    regioselective synthesis of 1,5-disubstituted tetrazoles has been developed. By means of electrophilic amide activation, and further C–C bond cleavage and rearrangement, a diverse set of functionalized 1,5-DST derivatives were selectively constructed under mild conditions. As showcased in the mechanisms, the chemoselectivity is easily switched by the selection of the starting materials in the reaction.
    开发了一种无属的全新的一锅多酰胺酰胺,用于化学和区域选择性合成1,5-二取代的四唑。通过亲电酰胺的活化,以及进一步的C–C键裂解和重排,在温和条件下选择性地构建了多种功能化的1,5-DST衍生物。如机理所示,通过选择反应中的起始原料可以容易地切换化学选择性。
  • Improved Schmidt Synthesis of 1,5-Disubstituted 1<i>H</i>-Tetrazoles from Ketones
    作者:Hitomi Suzuki、Young Seok Hwang、Chie Nakaya、Yoshihiro Matano
    DOI:10.1055/s-1993-26027
    日期:——
    On treatment with an excess of sodium azide in the presence of titanium(IV) chloride in boiling acetonitrile, both aliphatic and aromatic ketones are smoothly converted to 1,5-disubstituted 1H-tetrazoles in high yields.
    在沸腾的乙腈中,在(IV)的存在下,用过量叠氮进行处理,脂肪酮和芳香酮都能顺利转化为 1,5-二取代的 1H-四唑,产量很高。
  • The Effect of Some Substituents on the Thermal Breakdown of Diaryltetrazoles<sup>1</sup>
    作者:JOHN VAUGHAN、PETER A. S. SMITH
    DOI:10.1021/jo01106a023
    日期:1958.12
  • Direct C−H Arylation and Alkenylation of 1-Substituted Tetrazoles: Phosphine As Stabilizing Factor
    作者:Marcel Špulák、Richard Lubojacký、Petr Šenel、Jiří Kuneš、Milan Pour
    DOI:10.1021/jo902180u
    日期:2010.1.1
    Direct arylation and alkenylation of 1-substituted tetrazoles was achieved via Pd catalysis in the presence of CuI and CS2CO3. Unlike the related reactions of imidazoles and purines, phosphine ligand was necessary to prevent the intermediate tetrazolyl-Pd-II species from fragmentation into the corresponding cyanamide, Various 1,5-disubstituted tetrazoles were prepared with good to excellent isolated yields.
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