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3-mercapto-1,2,4-triazine

中文名称
——
中文别名
——
英文名称
3-mercapto-1,2,4-triazine
英文别名
1,2,4-triazine-3-thiol;2H-1,2,4-triazine-3-thione
3-mercapto-1,2,4-triazine化学式
CAS
——
化学式
C3H3N3S
mdl
——
分子量
113.143
InChiKey
SOFPIAMTOZWXKT-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
  • 重原子数:
    7
  • 可旋转键数:
    0
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    68.8
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    3-mercapto-1,2,4-triazine2-二乙氨基-1-溴乙烷氢溴酸盐N,N-二异丙基乙胺 作用下, 以 2,4-滴二甲胺盐 为溶剂, 反应 2.0h, 以10%的产率得到2-(1,2,4-triazin-3-ylthio)-N,N-diethylethan-1-amine
    参考文献:
    名称:
    3-Alkylthio-1,2,4-triazine dimers with potent antimalarial activity
    摘要:
    We report on the discovery of 3-alkylthio-1,2,4-triazine dimers that are potently toxic to Plasmodium falciparum, with single digit nanomolar activity, and up to several thousand-fold lower toxicity to mammalian cells. They are equipotent against chloroquine-resistant strains of P. falciparum. (c) 2010 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2010.08.065
  • 作为产物:
    描述:
    草酸醛氨基硫脲 反应 0.12h, 以93%的产率得到3-mercapto-1,2,4-triazine
    参考文献:
    名称:
    在无溶剂系统中微波辐照下使用氨基硫脲一锅法合成一些氮和硫杂环
    摘要:
    在微波辐射下,在无溶剂体系中以极短的时间以极好的收率合成了噻唑酮、三嗪和三嗪酮。
    DOI:
    10.1080/104265090968992
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文献信息

  • One-Pot Synthesis of Some Nitrogen and Sulfur Heterocycles Using Thiosemicarbazide Under Microwave Irradiation in a Solventless System
    作者:Majid M. Heravi、Navabeh Nami、Hossien A. Oskooie、Rahim Hekmatshoar
    DOI:10.1080/104265090968992
    日期:2006.1.1
    A thiazolon, triazines, and triazinones were synthesized under microwave irradiation in a solventless system in a very short time and in excellent yields.
    在微波辐射下,在无溶剂体系中以极短的时间以极好的收率合成了噻唑酮、三嗪和三嗪酮。
  • Substituted [(Phenylethanoyl)Amino]Benzamides
    申请人:Bruggemeier Ulf
    公开号:US20080171786A1
    公开(公告)日:2008-07-17
    The invention relates to substituted [(phenylethanoyl)amino]benzamides and methods for their preparation, and their use for the manufacture of medicaments for the treatment and/or prophylaxis of diseases, in particular of inflammatory disorders such as, for example, cutaneous, respiratory tract and cardiovascular disorders such as, for example, arteriosclerosis and coronary heart disease.
    本发明涉及取代的[(苯乙酰)氨基]苯甲酰胺及其制备方法,以及它们用于制造药物,用于治疗和/或预防疾病,特别是炎症性疾病,例如皮肤、呼吸道和心血管疾病,例如动脉硬化和冠心病。
  • Substituted [(phenylethanoyl)amino]benzamides
    申请人:Bayer Schering Pharma Aktiengesellschaft
    公开号:US07776922B2
    公开(公告)日:2010-08-17
    The invention relates to substituted [(phenylethanoyl)amino]benzamides and methods for their preparation, and their use for the manufacture of medicaments for the treatment and/or prophylaxis of diseases, in particular of inflammatory disorders such as, for example, cutaneous, respiratory tract and cardiovascular disorders such as, for example, arteriosclerosis and coronary heart disease.
    本发明涉及取代的[(苯乙酰)氨基]苯甲酰胺及其制备方法,以及它们用于制造治疗和/或预防疾病的药物,特别是用于治疗炎症性疾病,例如皮肤、呼吸道和心血管疾病,例如动脉硬化和冠心病。
  • 3-Alkylthio-1,2,4-triazine dimers with potent antimalarial activity
    作者:Kung Ban、Sandra Duffy、Yelena Khakham、Vicky M. Avery、Andrew Hughes、Oliver Montagnat、Kasiram Katneni、Eileen Ryan、Jonathan B. Baell
    DOI:10.1016/j.bmcl.2010.08.065
    日期:2010.10
    We report on the discovery of 3-alkylthio-1,2,4-triazine dimers that are potently toxic to Plasmodium falciparum, with single digit nanomolar activity, and up to several thousand-fold lower toxicity to mammalian cells. They are equipotent against chloroquine-resistant strains of P. falciparum. (c) 2010 Elsevier Ltd. All rights reserved.
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