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2-(3,5-dichlorophenylthio)aniline | 1375830-03-7

中文名称
——
中文别名
——
英文名称
2-(3,5-dichlorophenylthio)aniline
英文别名
2-(3,5-Dichlorophenyl)sulfanylaniline;2-(3,5-dichlorophenyl)sulfanylaniline
2-(3,5-dichlorophenylthio)aniline化学式
CAS
1375830-03-7
化学式
C12H9Cl2NS
mdl
——
分子量
270.182
InChiKey
DZBYTHSGWVDSAC-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):
    4.6
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    51.3
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    苯并噻唑3,5-二氯碘苯四丁基氢氧化铵copper(l) chloride 作用下, 反应 12.0h, 以85%的产率得到2-(3,5-dichlorophenylthio)aniline
    参考文献:
    名称:
    Unexpectedly ligand-free copper-catalyzed C–S cross-coupling of benzothiazole with aryl iodides in aqueous solution
    摘要:
    A novel synthetic protocol for 2-aminophenyl sulfide derivatives via the reactions of benzothiazole with aryl iodides was reported for the first time. The reactions were catalyzed by CuCl with tetrabutylammonium hydroxide as the base and water as the solvent without ligand at 50 degrees C or room temperature. A variety of aryl iodides underwent the C-S cross-coupling reaction with benzothiazole to afford smoothly the corresponding products in excellent yield. (C) 2012 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2012.04.004
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文献信息

  • Unexpectedly ligand-free copper-catalyzed C–S cross-coupling of benzothiazole with aryl iodides in aqueous solution
    作者:Yi-Si Feng、Hong-Xia Qi、Wei-Cheng Wang、Yu-Feng Liang、Hua-Jian Xu
    DOI:10.1016/j.tetlet.2012.04.004
    日期:2012.6
    A novel synthetic protocol for 2-aminophenyl sulfide derivatives via the reactions of benzothiazole with aryl iodides was reported for the first time. The reactions were catalyzed by CuCl with tetrabutylammonium hydroxide as the base and water as the solvent without ligand at 50 degrees C or room temperature. A variety of aryl iodides underwent the C-S cross-coupling reaction with benzothiazole to afford smoothly the corresponding products in excellent yield. (C) 2012 Elsevier Ltd. All rights reserved.
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