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4-methyl-5-(naphthalen-1-yl)-2-phenyl-1H-imidazole

中文名称
——
中文别名
——
英文名称
4-methyl-5-(naphthalen-1-yl)-2-phenyl-1H-imidazole
英文别名
2-Phenyl-4-(1-naphthyl)-5-methylimidazole;5-methyl-4-naphthalen-1-yl-2-phenyl-1H-imidazole
CAS
——
化学式
C20H16N2
mdl
——
分子量
284.36
InChiKey
INQRDWQKHMKYTQ-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):
    5
  • 重原子数:
    22
  • 可旋转键数:
    2
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.05
  • 拓扑面积:
    28.7
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    苯甲腈copper (I) acetate氯化铵 作用下, 以 甲醇二甲基亚砜 为溶剂, 反应 84.0h, 生成 4-methyl-5-(naphthalen-1-yl)-2-phenyl-1H-imidazole
    参考文献:
    名称:
    以碳化钙为炔烃源通过A3-偶联环化构建5-甲基-2,4-二芳基-1H-咪唑
    摘要:
    咪唑衍生物是合成药物、荧光材料和配体的关键组成部分。尽管开发了许多策略,但 2,4,5-取代咪唑的可靠合成仍在大量研究中。在这项研究中,我们提出了一种合成 2,4,5-取代咪唑甲基的方案,使用 A3 偶联环化与碳化钙作为乙炔源,与脒和醛反应。该方法具有几个特点,包括使用固体炔烃源、易于获取的起始材料以及对 34 个示例的适用性。
    DOI:
    10.1002/adsc.202300221
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文献信息

  • [EN] PHENYLNAPHTHYLIMIDAZOLES FOR USE ON COPPER SURFACES DURING SOLDERING<br/>[FR] PHÉNYLNAPHTHYLIMIDAZOLES EN VUE D'UNE UTILISATION SUR LES SURFACES EN CUIVRE AU COURS D'UN BRASAGE
    申请人:SHIKOKU CHEM
    公开号:WO2005121101A1
    公开(公告)日:2005-12-22
    A surface treating agent containing a novel phenylnaphthylimidazole compound represented by the following formula is brought into contact with the surface of copper or a copper alloy. In the formula, when A1 is a phenyl group, then A2 represents a 1-naphthyl group or a 2-naphthyl group, and when A1 is a 1-naphthyl group or a 2-naphthyl group, then A2 represents a phenyl group; and R represents a hydrogen atom or a methyl group.
    含有所述下列公式表示的新型苯基咪唑啉化合物的表面处理剂与的表面接触。在公式中,当A1是苯基时,A2代表1-基或2-基,当A1是1-基或2-基时,A2代表苯基;R代表氢原子或甲基。
  • Phenylnaphthylimidazole Compound and Usage of the Same
    申请人:Hirao Hirohiko
    公开号:US20070246134A1
    公开(公告)日:2007-10-25
    A surface treating agent containing a novel phenylnaphthylimidazole compound represented by the following formula is brought into contact with the surface of copper or a copper alloy. In the formula, when A 1 is a phenyl group, then A 2 represents a 1-naphthyl group or a 2-naphthyl group, and when A 1 is a 1-naphthyl group or a 2-naphthyl group, then A 2 represents a phenyl group; and R represents a hydrogen atom or a methyl group.
    一种表面处理剂,其含有一种新的苯基咪唑化合物,其化学式如下,与的表面接触。在该式中,当A1为苯基时,A2表示1-基或2-基,当A1为1-基或2-基时,A2表示苯基;R表示氢原子或甲基基团。
  • PHENYLNAPHTHYLIMIDAZOLE COMPOUND AND USAGE OF THE SAME
    申请人:Hirao Hirohiko
    公开号:US20120199385A1
    公开(公告)日:2012-08-09
    A surface treating agent containing a novel phenylnaphthylimidazole compound represented by the following formula is brought into contact with the surface of copper or a copper alloy. In the formula, when A 1 is a phenyl group, then A 2 represents a 1-naphthyl group or a 2-naphthyl group, and when A 1 is a 1-naphthyl group or a 2-naphthyl group, then A 2 represents a phenyl group; and R represents a hydrogen atom or a methyl group.
    一种表面处理剂,包含以下公式所表示的新型苯基咪唑化合物,与的表面接触。在公式中,当A1为苯基时,A2代表1-基或2-基,当A1为1-基或2-基时,A2代表苯基;而R代表氢原子或甲基基团。
  • Phenylnaphthylimidazole compound and usage of the same
    申请人:Hirao Hirohiko
    公开号:US08378116B2
    公开(公告)日:2013-02-19
    A surface treating agent containing a novel phenylnaphthylimidazole compound represented by the following formula is brought into contact with the surface of copper or a copper alloy. In the formula, when A1 is a phenyl group, then A2 represents a 1-naphthyl group or a 2-naphthyl group, and when A1 is a 1-naphthyl group or a 2-naphthyl group, then A2 represents a phenyl group; and R represents a hydrogen atom or a methyl group.
    一种含有新型苯基咪唑化合物的表面处理剂与的表面接触。在公式中,当A1为苯基时,A2代表1-基或2-基,当A1为1-基或2-基时,A2代表苯基;R代表氢原子或甲基基团。
  • PHENYLNAPHTHYLIMIDAZOLES FOR USE ON COPPER SURFACES DURING SOLDERING
    申请人:SHIKOKU CHEMICALS CORPORATION
    公开号:EP1753728A1
    公开(公告)日:2007-02-21
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