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(ethylsulfanyl-methyl)-dimethyl-amine | 117409-99-1

中文名称
——
中文别名
——
英文名称
(ethylsulfanyl-methyl)-dimethyl-amine
英文别名
(Aethylmercapto-methyl)-dimethyl-amin;Dimethylaminomethyl-aethyl-sulfid;1-ethylsulfanyl-N,N-dimethylmethanamine
(ethylsulfanyl-methyl)-dimethyl-amine化学式
CAS
117409-99-1
化学式
C5H13NS
mdl
——
分子量
119.231
InChiKey
YDYIHRYOSYCPNC-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):
    1.4
  • 重原子数:
    7
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    28.5
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    triethylsiloxymethyl-N,N-dimethylamine 、 乙硫醇 以67%的产率得到(ethylsulfanyl-methyl)-dimethyl-amine
    参考文献:
    名称:
    三乙基甲硅烷氧基甲基-NN-二甲基胺,Et3SiOCH2NMe2:一种用于OH,SH,PH和芳族CH体系的新型二甲基氨基甲基化(Mannich)试剂
    摘要:
    三乙基甲硅烷氧基甲基胺Et3SiOCH2NMe2易于通过Et3SiH和DMF之间的氢化硅烷化反应以高收率制备,对于脂族醇,硫醇和Ph2PH(EH)材料的代表性范围而言,它是一种出色的(N,N-二甲基氨基)甲基转移剂。反应在室温下在惰性溶剂中几乎是瞬时的,不需要活化剂即可高产率生产E-CH2NMe2产品,并说明标题化合物是有机试剂家族的绝佳添加。对于芳族醇,芳族官能团的亲电子取代以高收率发生。报道了诸如胆甾醇基-CH 2 NMe 2衍生物,2-4-4- [双(N,N-二甲基氨基)甲基] -1-萘酚和衍生自Ph 2 PCH 2 NMe 2的氧化膦的新材料的晶体结构。
    DOI:
    10.1002/ejoc.201700902
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文献信息

  • Renshaw; Searle, Journal of the American Chemical Society, 1937, vol. 59, p. 2057
    作者:Renshaw、Searle
    DOI:——
    日期:——
  • Triethylsiloxymethyl-<i>N</i>,<i>N</i>-dimethylamine, Et<sub>3</sub>SiOCH<sub>2</sub>NMe<sub>2</sub>: A Dimethylaminomethylation (Mannich) Reagent for O-H, S-H, P-H and Aromatic C-H Systems
    作者:Paulina E. Gonzalez、Hemant K. Sharma、Sanchita Chakrabarty、Alejandro Metta-Magaña、Keith H. Pannell
    DOI:10.1002/ejoc.201700902
    日期:2017.10.10
    Et3SiOCH2NMe2, readily made in high yield by the hydrosilylation reaction between Et3SiH and DMF, is an excellent (N,N-dimethylamino)methyl transfer agent to a representative range of aliphatic alcohol, thiol and Ph2PH (E-H) materials. The reactions are almost instantaneous at room temperature in inert solvents and require no activating agents to produce E-CH2NMe2 products in high yield and illustrate the
    三乙基甲硅烷氧基甲基胺Et3SiOCH2NMe2易于通过Et3SiH和DMF之间的氢化硅烷化反应以高收率制备,对于脂族醇,硫醇和Ph2PH(EH)材料的代表性范围而言,它是一种出色的(N,N-二甲基氨基)甲基转移剂。反应在室温下在惰性溶剂中几乎是瞬时的,不需要活化剂即可高产率生产E-CH2NMe2产品,并说明标题化合物是有机试剂家族的绝佳添加。对于芳族醇,芳族官能团的亲电子取代以高收率发生。报道了诸如胆甾醇基-CH 2 NMe 2衍生物,2-4-4- [双(N,N-二甲基氨基)甲基] -1-萘酚和衍生自Ph 2 PCH 2 NMe 2的氧化膦的新材料的晶体结构。
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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