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1-(3-(甲基磺酰基)苯基)哌嗪盐酸盐 | 1352305-13-5

中文名称
1-(3-(甲基磺酰基)苯基)哌嗪盐酸盐
中文别名
——
英文名称
1-(3-methanesulfonylphenyl)piperazine hydrochloride
英文别名
1-(3-(Methylsulfonyl)phenyl)piperazine hydrochloride;1-(3-methylsulfonylphenyl)piperazine;hydrochloride
1-(3-(甲基磺酰基)苯基)哌嗪盐酸盐化学式
CAS
1352305-13-5
化学式
C11H16N2O2S*ClH
mdl
MFCD20921645
分子量
276.787
InChiKey
MLUWQKOMTQINGK-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):
    0.39
  • 重原子数:
    17
  • 可旋转键数:
    2
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.454
  • 拓扑面积:
    57.8
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为产物:
    描述:
    3-甲砜基苯胺二(2-氯乙基)胺盐酸盐环丁砜 为溶剂, 反应 14.0h, 以92%的产率得到1-(3-(甲基磺酰基)苯基)哌嗪盐酸盐
    参考文献:
    名称:
    An efficient scale up process for synthesis of N-arylpiperazines
    摘要:
    An efficient protocol for the synthesis of various substituted phenylpiperazines was developed using sulfolane as solvent. The protocol was clean, high yielding and products were obtained in high purities (>= 99%). It was also fast and convenient, as the final products were precipitated as hydrochloride salts and could be obtained by filtration. Sulfolane, an aprotic, dipolar, high boiling and recoverable solvent was used as a substitute for common organic solvents. (C) 2015 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2015.06.003
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文献信息

  • An efficient scale up process for synthesis of N-arylpiperazines
    作者:Lokesh Ravilla、N. Venkata Subba Naidu、Kuppuswamy Nagarajan
    DOI:10.1016/j.tetlet.2015.06.003
    日期:2015.7
    An efficient protocol for the synthesis of various substituted phenylpiperazines was developed using sulfolane as solvent. The protocol was clean, high yielding and products were obtained in high purities (>= 99%). It was also fast and convenient, as the final products were precipitated as hydrochloride salts and could be obtained by filtration. Sulfolane, an aprotic, dipolar, high boiling and recoverable solvent was used as a substitute for common organic solvents. (C) 2015 Elsevier Ltd. All rights reserved.
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