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N'-butylhydrazinecarbodithioic acid hexyl ester | 1138320-54-3

中文名称
——
中文别名
——
英文名称
N'-butylhydrazinecarbodithioic acid hexyl ester
英文别名
N'-butylhydrazinecarbodithioic acid n-hexyl ester;hexyl 2-butylhydrazinecarbodithioate;Hexyl 2-butylhydrazinecarbodithioate;hexyl N-(butylamino)carbamodithioate
N'-butylhydrazinecarbodithioic acid hexyl ester化学式
CAS
1138320-54-3
化学式
C11H24N2S2
mdl
——
分子量
248.457
InChiKey
MLTQLFRBKBKZRK-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):
    4.4
  • 重原子数:
    15
  • 可旋转键数:
    10
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.91
  • 拓扑面积:
    81.4
  • 氢给体数:
    2
  • 氢受体数:
    3

反应信息

  • 作为产物:
    描述:
    二硫化碳丁基肼1-氯己烷苄基三甲基氢氧化铵 作用下, 以 neat (no solvent) 为溶剂, 反应 3.0h, 以95%的产率得到N'-butylhydrazinecarbodithioic acid hexyl ester
    参考文献:
    名称:
    Triton-B催化绿色高效合成二硫代氨基甲酸酯的方法
    摘要:
    一种新颖的无溶剂高产率的方法被成功实现,用于通过不同烷基卤化物(初级、次级和三级)与多种取代肼的反应,进行一步法合成二硫 Carbazates,所使用的试剂为 Triton-B(苄基三甲基铵氢氧化物)和二硫化碳。与之前采用的方法相比,这种新方法在合成二硫 Carbazates 方面具有温和的反应条件、简单的操作过程和高产率的优势。
    DOI:
    10.14233/ajchem.2019.21973
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文献信息

  • An efficient one-pot synthesis of carbazates and dithiocarbazates through the corresponding alcohols using Mitsunobu’s reagent
    作者:A. K. Chaturvedi、D. Chaturvedi、N. Mishra、V. Mishra
    DOI:10.1007/bf03249073
    日期:2011.6
    A novel Mitsunobu-based protocol has been developed for the synthesis of carbazates and dithiocarbazates through the variety of corresponding primary, secondary and tertiary alcohols and various kinds of substituted hydrazines using Mitsunobu’s reagent and CO2/CS2 system, in good to excellent yields.
    使用Mitsunobu的试剂和CO 2 / CS 2系统,已开发出一种新颖的基于Mitsunobu的新方案,可通过使用Mitsunobu的试剂和CO 2 / CS 2系统通过各种相应的伯醇,仲醇和叔醇以及各种取代的来合成氨基甲酸酯和二氨基甲酸酯。
  • An Efficient, Basic Resin-Mediated, One-Pot Synthesis of Dithiocarbazates Through Alcoholic Tosylates
    作者:Devdutt Chaturvedi、Nisha Mishra、Amit K. Chaturvdi、Virendra Mishra
    DOI:10.1080/10426500802203137
    日期:2009.3.10
    A quick and efficient, one-pot synthesis of dithiocarbazates was accomplished in high yields by the reaction of various alcoholic tosylates of primary, secondary, and tertiary alcohols, with substituted hydrazines using an Amberlite IRA 400 (basic resin)/CS2 system. The reaction conditions are mild with simpler work-up procedures than previously reported methods.
  • Triton-B-Catalyzed, Efficient, One-Pot Synthesis of Dithiocarbazates Through Alcoholic Tosylates
    作者:Devdutt Chaturvedi、Nisha Mishra、Amit K. Chaturvedi、Virendra Mishra
    DOI:10.1080/00397910802519141
    日期:2009.3.10
    A quick, efficient, one-pot synthesis of dithiocarbazates was accomplished in high yields by the reaction of various tosylates of primary, secondary, and tertiary alcohols with a variety of substituted hydrazines using the benzyl-trimethylammonium hydroxide (Triton-B)/CS2 system. The reaction conditions are mild with simpler workup procedures than the reported methods.
  • Triton-B catalyzed, efficient one-pot synthesis of dithiocarbazates
    作者:Devdutt Chaturvedi、Nisha Mishra、Virendra Mishra
    DOI:10.1007/s00706-008-0873-9
    日期:2008.9
    A quick and efficient, one-pot synthesis of dithiocarbazates was accomplished in high yields by the reaction of various primary, secondary, and tert. alkyl halides with a variety of substituted hydrazines using the benzyl-trimethylammonium hydroxide (Triton-B)/CS2 system. The reaction conditions are mild with simpler work-up procedures than the reported methods.
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