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sodium salt of 5-phenyltetrazole | 29814-09-3

中文名称
——
中文别名
——
英文名称
sodium salt of 5-phenyltetrazole
英文别名
sodium;5-phenyl-1,2,3-triaza-4-azanidacyclopenta-2,5-diene
sodium salt of 5-phenyltetrazole化学式
CAS
29814-09-3
化学式
C7H5N4*Na
mdl
——
分子量
168.133
InChiKey
CSWZYKIBOAGLMW-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):
    -2.5
  • 重原子数:
    12.0
  • 可旋转键数:
    1.0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    52.77
  • 氢给体数:
    0.0
  • 氢受体数:
    3.0

反应信息

点击查看最新优质反应信息

文献信息

  • Synthesis and antiviral activity of nonannulated tetrazolylpyrimidines
    作者:Vladimir А. Ostrovskii、Gevorg G. Danagulyan、Olga M. Nesterova、Yulia N. Pavlyukova、Vladimir V. Tolstyakov、Olga S. Zarubina、Pavel А. Slepukhin、Yana L. Esaulkova、Anna А. Muryleva、Vladimir V. Zarubaev、Rostislav E. Trifonov
    DOI:10.1007/s10593-021-02922-6
    日期:2021.4
    tetrazolylpyrimidines in the structure of which the heterocyclic fragments are separated by hydrazinocarbonylmethyl, methylpyrazolyl groups or a sulfur atom were synthesized. Some of these compounds showed moderate in vitro activity against H1N1 subtype of influenza A virus. The selectivity index of the anti-influenza action of 5-[(4,6-dimethylpyrimidin-2-yl)sulfanyl]-1H-tetrazol-1-yl}acetic acid, which
    合成了结构中杂环片段被基羰基甲基、甲基吡唑基或原子分隔的非环化四唑嘧啶。其中一些化合物对甲型流感病毒 H1N1 亚型表现出中等的体外活性。细胞毒性极低的5-[(4,6-二甲基嘧啶-2-基)基]-1 H-四唑-1-基}乙酸的抗流感作用选择性指数是其两倍作为对照药乙胺的选择性指标。
  • [EN] A PROCESS FOR THE PREPARATION OF PHENYLTETRAZOLE DERIVATIVES<br/>[FR] PROCEDE DE PREPARATION DE DERIVES DE PHENYLTETRAZOLE
    申请人:DIPHARMA SPA
    公开号:WO2005014560A1
    公开(公告)日:2005-02-17
    A process for the preparation of phenyltetrazole derivatives of formula (II) wherein R and Y are as defined in the disclosure, by direct ortho-metallation of (tetrazol-5-Ϝl)benzene. The compounds of formula (II) are useful intermediates for the preparation of angiotensin II antagonists.
    一种制备式(II)中R和Y如披露所定义的苯基四唑生物的过程,通过对(四唑-5-Ϝl)苯直接进行正交-属化。式(II)化合物是制备血管紧张素II拮抗剂的有用中间体。
  • Early Transition Metal Complexes Containing 1,2,4-Triazolato and Tetrazolato Ligands:  Synthesis, Structure, and Molecular Orbital Studies
    作者:Carlos Yélamos、Karl R. Gust、Anwar G. Baboul、Mary Jane Heeg、H. Bernhard Schlegel、Charles H. Winter
    DOI:10.1021/ic0109389
    日期:2001.12.1
    (tBu(2)pz = 3,5-di-tert-butylpyrazolato; x = 1, 2) and M(tBu(2)pz)(5-x)Cl(x) (M = Nb, Ta: x = 2, 3) with the sodium or potassium salts derived from 1,2,4-triazoles and tetrazoles. The X-ray structure analysis of Ti(tBu(2)pz)(2)(Me(2)C(2)N(3))(2) shows eta(2)-coordination of the 1,2,4-triazolato ligands, while in Ti(tBu(2)pz)(3)(C(2)H(2)N(3)) and Nb(tBu(2)pz)(3)(Me(2)C(2)N(3))(2) the analogous groups are
    通过吡唑并酮配合物Ti(tBu(2)pz)(4-x)Cl(x)(tBu(2)pz = 3)的反应已制备了几种带有1,2,4-三唑四唑配体的早期过渡属配合物,5-二叔丁基吡唑并(x = 1,2)和M(tBu(2)pz)(5-x)Cl(x)(M = Nb,Ta:x = 2,3)与或由1,2,4-三唑四唑衍生的盐。Ti(tBu(2)pz)(2)(Me(2)C(2)N(3))(2)的X射线结构分析显示1,2,4-的eta(2)配位Triazolato配体,而在Ti(tBu(2)pz)(3)(C(2)H(2)N(3))和Nb(tBu(2)pz)(3)(Me(2)C(2 )N(3))(2)的类似基团以固态结构的eta(1)形式连接。在不同温度下的溶液NMR研究表明,固态包含eta(1)-1,2,4-三唑配体的配合物涉及eta(2)-1,2,4-三唑配体的过渡态。类似的四唑络合物Ti(t
  • An Electron-Deficient Coordination Polymer Based on a Viologen Ligand Accompanying Photochromism, Vaporchromism, and Photoswitchable Luminescence Properties
    作者:S. X. Cui、Q. Z. Yin、J. H. Yu、J. Jiang、Y. C. Zou
    DOI:10.1134/s0036023620060042
    日期:2020.6
    AbstractA novel viologen ligand, 1,1'-bis-(4-carboxybenzyl)-4,4'-bipyridinium- dibromide (H2BpybcBr2), has been synthesized and successfully introduced into cadmium based coordination polymers (CPs) when it reacts with cadmium perchlorate and 5-phenyltetrazole (5-Ph-Ptz) at room temperature. CPs has been characterized with single-crystal X-ray diffraction, powder X-ray diffraction, and thermogravimetric
    摘要一种新型的紫精配体1,1'-双-(4-羧基苄基)-4,4'-联吡啶-二化物(H 2 BpybcBr 2)已合成,并在其反应时成功引入了基配位聚合物(CPs)中。在室温下用高氯酸镉和5-苯基四唑(5-Ph-Ptz)混合。CP的特征在于单晶X射线衍射,粉末X射线衍射和热重分析。CP 1对紫外线可见辐射具有高灵敏度,并具有电子转移(ET)光致变色特性。有趣的是,CP 1在着色-脱色过程中表现出光控发光特性,可用于检测固态的苯胺
  • New ring-transformation reaction: the conversion of a tetrazole ring into a 1-oxa-3,4-diazine ring
    作者:Aleksei B. Sheremetev、Natal’ya S. Aleksandrova、Kyrill Yu. Suponitsky、Mikhail Yu. Antipin
    DOI:10.1016/j.mencom.2009.03.012
    日期:2009.3
    New ring cleavage/ring closure reactions of tetrazole derivatives provide a route to a new heterocyclic system such as furazano[3,4-e]-1-oxa-3,4-diazine, which was characterized by 1H, 13C and 14N NMR spectroscopy and X-ray crystallography.
    四唑生物的新的开环裂解/闭环反应提供了通往新的杂环体系的途径,例如呋喃并[3,4-e] -1-oxa-3,4-diazine,其特征在于1H,13C和14N NMR光谱和X射线晶体学。
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