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S-甲基叔丁基硫代氨基甲酸酯 | 100367-95-1

中文名称
S-甲基叔丁基硫代氨基甲酸酯
中文别名
——
英文名称
S-methyl tert-butylthiocarbamate
英文别名
Methyl tert-butylthiocarbamate;tert-butyl-thiocarbamic acid S-methyl ester;tert-Butyl-thiocarbamidsaeure-S-methylester;S-methyl N-tert-butylcarbamothioate
S-甲基叔丁基硫代氨基甲酸酯化学式
CAS
100367-95-1
化学式
C6H13NOS
mdl
——
分子量
147.241
InChiKey
KEQPYCLRZOAMEC-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):
    1.5
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    54.4
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    参考文献:
    名称:
    Three-component cyclocondensations. Two methods for the efficient preparation of 5-aminothiazolium salts via the reaction of isocyanides either with dimethylthioformamide and imino chloro sulfides or benzaldimines and aryl chlorothioformates
    摘要:
    Treatment of imino chloro sulfides with dimethylthioformamide and isocyanides at room temperature provides selectively the 5-amino-4-(dimethylamino)-2-(methylthio)(or phenylthio)thiazolium salts. Similarly, the reactions of p-tolyl chlorothionoformate and phenyl chlorodithioformate with a mixture of benzaldimine and isocyanide afford rapidly the 5-amino-4-phenylthiazolium salts. We suggest that these reactions involve the N-(thiocarbonyl)formamidinium and benzylideniminium chlorides as transient intermediates, which are trapped by isocyanides according to a [1 + 4] cycloaddition process. The structure of the thiazolium salts and some of their reactivities are discussed.
    DOI:
    10.1021/jo00074a032
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文献信息

  • Iodide-Catalyzed Synthesis of Secondary Thiocarbamates from Isocyanides and Thiosulfonates
    作者:Pieter Mampuys、Yanping Zhu、Sergey Sergeyev、Eelco Ruijter、Romano V. A. Orru、Sabine Van Doorslaer、Bert U. W. Maes
    DOI:10.1021/acs.orglett.6b01023
    日期:2016.6.17
    A new method for the synthesis of secondary thiocarbamates from readily available isocyanides and thiosulfonates with broad functional group tolerance is reported. The reaction proceeds under mild reaction conditions in isopropanol and is catalyzed by inexpensive sodium iodide.
    报道了一种从易得的异氰酸酯和具有宽泛的官能团耐受性的磺酸盐合成仲氨基甲酸酯的新方法。该反应在温和的反应条件下在异丙醇中进行,并由廉价的碘化钠催化。
  • Thiocarbamate und verwandte Verbindungen. Mitteilung IX: N-substituierte Monothiocarbamids�ure-S-R1-ester
    作者:R. Riemschneider、A. K�hl
    DOI:10.1007/bf00904150
    日期:——
  • Thiocarbamates and Related Compounds. X.<sup>1</sup> a New Reaction of Thiocyanates
    作者:Randolph Riemschneider
    DOI:10.1021/ja01585a038
    日期:1956.2
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