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N'-butylhydrazinecarbodithioic acid decyl ester | 1138320-56-5

中文名称
——
中文别名
——
英文名称
N'-butylhydrazinecarbodithioic acid decyl ester
英文别名
decyl 2-butylhydrazinecarbodithiolate;N'-butylhydrazinecarbodithioic acid n-decyl ester;decyl 2-butylhydrazinecarbodithioate;Decyl 2-butylhydrazinecarbodithioate;decyl N-(butylamino)carbamodithioate
N'-butylhydrazinecarbodithioic acid decyl ester化学式
CAS
1138320-56-5
化学式
C15H32N2S2
mdl
——
分子量
304.564
InChiKey
XRKOJVQJAMBIFW-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

物化性质

  • 熔点:
    120 °C
  • 沸点:
    390.7±25.0 °C(predicted)
  • 密度:
    0.973±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.6
  • 重原子数:
    19
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.93
  • 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:
    二硫化碳丁基肼癸醇三苯基膦偶氮二甲酸二乙酯 作用下, 以 二甲基亚砜 为溶剂, 反应 1.5h, 以98%的产率得到N'-butylhydrazinecarbodithioic acid decyl ester
    参考文献:
    名称:
    使用Mitsunobu试剂通过相应的醇有效地一锅法合成氨基甲酸酯和二硫代氨基甲酸酯
    摘要:
    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肼来合成氨基甲酸酯和二硫代氨基甲酸酯。
    DOI:
    10.1007/bf03249073
点击查看最新优质反应信息

文献信息

  • Triton-B Catalyzed, Green and Efficient Method for the Synthesis of Dithiocarbazates
    作者:Sadaf Zaidi、Mridula Saxena
    DOI:10.14233/ajchem.2019.21973
    日期:2019.6.10
    A novel, solvent free and high yielding method was accomplished for one-pot synthesis of dithiocarbazates by the reaction of various alkyl halides (primary, secondary and tertiary) with variety of substituted hydrazines using Triton-B (benzyl-trimethylammonium hydroxide) and carbon di sulphide. This new method of synthesizing dithiocarbazates involves mild conditions, simple procedures and high yields of the products as compared to previously used methods.
    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)与多种取代的反应,进行一步法合成二 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 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。
  • Efficient TBAI-CS<sub>2</sub> Promoted Synthesis of Substituted Hydrazinecarbodithiolates
    作者:Nitin Srivastava
    DOI:10.1080/00304948.2022.2111171
    日期:2022.11.2
    Published in Organic Preparations and Procedures International: The New Journal for Organic Synthesis (Vol. 54, No. 6, 2022)
    发表于国际有机制剂和程序:有机合成新期刊(印刷前,2022 年)
  • 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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