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2-[(Z)-(2-hydroxyphenyl)methylidene]-N,N-bis(phenylmethyl)hydrazine-1-carbothioamide | 1310677-62-3

中文名称
——
中文别名
——
英文名称
2-[(Z)-(2-hydroxyphenyl)methylidene]-N,N-bis(phenylmethyl)hydrazine-1-carbothioamide
英文别名
1,1-dibenzyl-3-[(Z)-(2-hydroxyphenyl)methylideneamino]thiourea
2-[(Z)-(2-hydroxyphenyl)methylidene]-N,N-bis(phenylmethyl)hydrazine-1-carbothioamide化学式
CAS
1310677-62-3
化学式
C22H21N3OS
mdl
——
分子量
375.494
InChiKey
MFJNHMAVFNZZBT-HAHDFKILSA-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):
    4.4
  • 重原子数:
    27
  • 可旋转键数:
    6
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.09
  • 拓扑面积:
    80
  • 氢给体数:
    2
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为产物:
    参考文献:
    名称:
    Novel antitubercular diallyl/dibenzylthiosemicarbazones endowed with high activity toward multi-drug-resistant tuberculosis
    摘要:
    Novel diallyl and dibenzylthiosemicarbazones were prepared by three-step reactions. The compounds were tested for their in vitro activity against Mycobacterium tuberculosis H37Rv (MTB) and multi-drug-resistant Mycobacterium tuberculosis (MDR-TB). Most of the compounds showed excellent activity toward MDR-TB. Among the thirty compounds (4,5a-o) tested N,N-dibenzyl-2-((5-nitrofuran-2-yl)methylene)hydrazinecarbothioamide (5g) was found to be the most potent compound MICs of 0.55 and 0.12 mu M against MTB and MDR-TB.
    DOI:
    10.1007/s00044-011-9638-9
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文献信息

  • Novel antitubercular diallyl/dibenzylthiosemicarbazones endowed with high activity toward multi-drug-resistant tuberculosis
    作者:Dharmarajan Sriram、Debjani Banerjee、Tara Sasank Thripuraribhatla Venkat Varuna、Manikandaprabu Sankar、Perumal Yogeeswari
    DOI:10.1007/s00044-011-9638-9
    日期:2012.6
    Novel diallyl and dibenzylthiosemicarbazones were prepared by three-step reactions. The compounds were tested for their in vitro activity against Mycobacterium tuberculosis H37Rv (MTB) and multi-drug-resistant Mycobacterium tuberculosis (MDR-TB). Most of the compounds showed excellent activity toward MDR-TB. Among the thirty compounds (4,5a-o) tested N,N-dibenzyl-2-((5-nitrofuran-2-yl)methylene)hydrazinecarbothioamide (5g) was found to be the most potent compound MICs of 0.55 and 0.12 mu M against MTB and MDR-TB.
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