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N-mercaptomethylformamide | 1142179-00-7

中文名称
——
中文别名
——
英文名称
N-mercaptomethylformamide
英文别名
N-(sulfanylmethyl)formamide
N-mercaptomethylformamide化学式
CAS
1142179-00-7
化学式
C2H5NOS
mdl
——
分子量
91.1338
InChiKey
URCQZPOORXEVKW-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):
    -0.1
  • 重原子数:
    5
  • 可旋转键数:
    1
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    30.1
  • 氢给体数:
    2
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    S-(formylamino)methyl thioacetate四氢吡咯 作用下, 以88%的产率得到N-mercaptomethylformamide
    参考文献:
    名称:
    一种简单高效的新型甲醛衍生物的制备
    摘要:
    通过短而通用的途径以高收率制备了新的甲醛衍生物。确定了相应的硫代乙酸酯和硫醇的几种晶体结构。在酸性或碱性条件下将硫代乙酸酯裂解,以高收率得到硫醇,从而引入了新的N-巯基甲基烷基甲酰胺类,N-巯基甲基磺酰胺类和烷氧基甲硫醇类物质。 N-巯甲基甲基酰胺-N-巯甲基磺酰胺-甲氧基甲硫醇
    DOI:
    10.1055/s-0028-1083305
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文献信息

  • A Simple and Efficient Preparation of Novel Formaldehyde Derivatives
    作者:Hans Pfaendler、Rainer Hartung、Gregor Golz、Susanne Schlaf、Gudrun Silvennoinen、Kurt Polborn、Peter Mayer
    DOI:10.1055/s-0028-1083305
    日期:——
    New formaldehyde derivatives were prepared in good yields by a short and versatile route. Several crystal structures of corresponding thioacetic acid esters and thiols were determined. The thioacetates were cleaved under acidic or basic conditions affording the thiols in high yield, thus introducing the new substance classes of N-mercaptomethyl-alkylcarboxamides, N-mercapto­methylsulfonamides, and
    通过短而通用的途径以高收率制备了新的甲醛衍生物。确定了相应的硫代乙酸酯和硫醇的几种晶体结构。在酸性或碱性条件下将硫代乙酸酯裂解,以高收率得到硫醇,从而引入了新的N-巯基甲基烷基甲酰胺类,N-巯基甲基磺酰胺类和烷氧基甲硫醇类物质。 N-巯甲基甲基酰胺-N-巯甲基磺酰胺-甲氧基甲硫醇
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同类化合物

N,N,N',N'-四(乙硫基甲基)乙二胺 1-氨基乙硫醇 tert.-octylthiomethylamine 3-butyl-1,5,3-dithiazepane N,N,4-trimethyl-1-(methylthio)-4-penten-2-yn-1-amine aminoethanethiol hydrochloride N-(tert.-butylthiomethyl)-N-methyl amine hydrochloride 2,3-bis-(acetylamino-methylsulfanyl)-propan-1-ol N-(α-mercaptoethyl)formamide 1-amino-4-methylthiobutane N,N-dimethylaminoethanethiol 3-(tert-butyl)perhydro-1,5,3-dithiazepine 2Cyclohexylamino-2-methylthio-1,1-ethylenedicarbonitrile N-[(Octylsulfanyl)methyl]-N-(prop-2-en-1-yl)prop-2-en-1-amine N-(Thiomethyl)thioglycolsaeureamid Diethyl-(3-triethylsilanyl-propylsulfanylmethyl)-amine [2-(Diethyl-methyl-silanyl)-ethylsulfanylmethyl]-diethyl-amine N-ethyl-N-(propan-2-ylsulfanylmethyl)ethanamine Dimethyl-(1-methylsulfanyl-allyl)-amine Methyl-formamidomethyl-sulfid 2-(Dimethylaminomethylsulfanyl)ethanol Methyl-diethylaminomethylsulfid N,N'-Dimethyl-N,N'-diethylthiomethyl-ethylendiamin (ethylsulfanyl-methyl)-dimethyl-amine N,N-diethylcarbamodithioic acid (2,2,2-trichloro-1-formamidoethyl) ester Bis-(N,N-dimethyl-methylamin)-sulfid Tris-methylthiomethyl-amin 1-N,N-dimethylamino-1-methylthio-5,5-dimethyl-2-cyclohexene-3-thiol N-Ethyl-N-({[2-(trimethylsilyl)ethyl]sulfanyl}methyl)ethanamine N-(methylsulfanylmethyl)acetamide N-Ethyl-N-({[3-(trimethylsilyl)propyl]sulfanyl}methyl)ethanamine 2,2,2-trichloro-N-<(methylthio)methyl>acetamide N-[[2-(acetamidomethylsulfanylmethyl)-3-hydroxypropyl]sulfanylmethyl]acetamide 2,2,2-trifluoro-N-mercaptomethylacetamide 1-(Propylsulfanyl)methanamine S-(formylamino)methyl thioacetate N-(methylsulfanylmethyl)propan-1-amine;hydrochloride 1-Aminoundecane-1-thiol N-Ethyl-N-({[2-(triethylsilyl)ethyl]sulfanyl}methyl)ethanamine Carbamic acid, dimethyldithio-, acetamidomethyl ester N,N-dimethyl-1-(methylthio)-2-heptyn-1-amine N,N-dimethyl-1-(methylthio)-4,4-diethoxy-2-butyn-1-amine N,N-dimethyl-1-(methylthio)-3-(cyclohex-1-yl)-2-propyn-1-amine Formamidomethyl-aethyl-sulfid N-(tert-butylsulfanylmethyl)formamide N-Dimethylaminomethyl-n-butylsulfid N1,N1,N8,N8-tetramethyl-2,7-dithiaoctane-1,8-diamine N-((2-hydroxyethylthio)methyl)acetamide [(Diethyl-methyl-silanyl)-methylsulfanylmethyl]-diethyl-amine ethyl thiomethyldiethylamine