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N-(methylsulfanylmethyl)acetamide | 83442-33-5

中文名称
——
中文别名
——
英文名称
N-(methylsulfanylmethyl)acetamide
英文别名
——
N-(methylsulfanylmethyl)acetamide化学式
CAS
83442-33-5
化学式
C4H9NOS
mdl
——
分子量
119.188
InChiKey
PATHDYUGQJLRIW-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):
    0.3
  • 重原子数:
    7
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 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:
    N-methylene acetamide 、 甲硫醇 生成 N-(methylsulfanylmethyl)acetamide
    参考文献:
    名称:
    LASNE, M. -C.;RIPOLL, J. -L.;THUILLIER, A., J. CHEM. RES. SYNOP, 1982, N 8, 214-215
    摘要:
    DOI:
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文献信息

  • Reaction of sulfoxides with nitriles in presence of trifluoracetic anhydride and trifluoroacetic acid : A case of ritter reaction on pummerer intermediate
    作者:Yashwant D. Vankar、C.Trinadha Rao
    DOI:10.1016/s0040-4020(01)96692-x
    日期:1985.1
    Reaction of various sulfoxides , with nitriles in presence of trifluoroacetic anhydride and trifluoroacetic acid gave the corresponding amides via a Ritter reaction on Pummerer intermediate derived from the sulfoxides.
    在三氟乙酸酐和三氟乙酸存在下,各种亚砜与腈反应,通过在衍生自亚砜的Pummerer中间体上进行Ritter反应,得到相应的酰胺。
  • VANKAR, YASHWANT, D.;TRINADHA, RAO, C., TETRAHEDRON, 1985, 41, N 16, 3405-3410
    作者:VANKAR, YASHWANT, D.、TRINADHA, RAO, C.
    DOI:——
    日期:——
  • LASNE, M. -C.;RIPOLL, J. -L.;THUILLIER, A., J. CHEM. RES. SYNOP, 1982, N 8, 214-215
    作者:LASNE, M. -C.、RIPOLL, J. -L.、THUILLIER, A.
    DOI:——
    日期:——
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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