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N-[2-(dimethylaminosulfanyl)ethylsulfanyl]-N-methylmethanamine | 24128-04-9

中文名称
——
中文别名
——
英文名称
N-[2-(dimethylaminosulfanyl)ethylsulfanyl]-N-methylmethanamine
英文别名
——
N-[2-(dimethylaminosulfanyl)ethylsulfanyl]-N-methylmethanamine化学式
CAS
24128-04-9
化学式
C6H16N2S2
mdl
——
分子量
180.338
InChiKey
ASPCJDHCVOCKAD-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):
    1.2
  • 重原子数:
    10
  • 可旋转键数:
    5
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    57.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • Organoaminosilanes and methods for making same
    申请人:Versum Materials US, LLC
    公开号:US10294250B2
    公开(公告)日:2019-05-21
    Organoaminosilanes, such as without limitation di-iso-propylaminosilane (DIPAS), are precursors for the deposition of silicon containing films such as silicon-oxide and silicon-nitride films. Described herein are methods to make organoaminosilane compounds, or other compounds such as organoaminodisilanes and organoaminocarbosilanes, via the catalytic hydrosilylation of an imine by a silicon source comprising a hydridosilane.
    有机氨基硅烷,例如但不限于二异丙氨基硅烷(DIPAS),是沉积氧化硅和氮化硅薄膜等含硅薄膜的前体。本文描述了通过包含氢基硅烷的硅源对亚胺进行催化氢硅烷化来制造有机氨基硅烷化合物或其他化合物如有机氨基二硅烷和有机氨基碳硅烷的方法。
  • Organoaminosilane precursors and methods for depositing films comprising same
    申请人:VERSUM MATERIALS US, LLC
    公开号:US10453675B2
    公开(公告)日:2019-10-22
    Described herein are precursors and methods for forming silicon-containing films. In one aspect, the precursor comprises a compound represented by one of following Formulae A through E below: In one particular embodiment, the organoaminosilane precursors are effective for a low temperature (e.g., 350° C. or less), atomic layer deposition (ALD) or plasma enhanced atomic layer deposition (PEALD) of a silicon-containing film. In addition, described herein is a composition comprising an organoaminosilane described herein wherein the organoaminosilane is substantially free of at least one selected from the amines, halides (e.g., Cl, F, I, Br), higher molecular weight species, and trace metals.
    本文描述了用于形成含硅薄膜的前体和方法。在一个方面,前驱体包括由下式 A 至 E 之一代表的化合物: 在一个特定的实施方案中,有机氨基硅烷前体对含硅薄膜的低温(如 350° C 或更低)、原子层沉积(ALD)或等离子体增强原子层沉积(PEALD)有效。此外,本文还描述了一种包含本文所述有机氨基硅烷的组合物,其中有机氨基硅烷基本上不含至少一种选自胺、卤化物(如Cl、F、I、Br)、高分子量物种和痕量金属的物质。
  • Organoaminosilanes and Methods for Making Same
    申请人:Versum Materials US, LLC
    公开号:US20170204120A1
    公开(公告)日:2017-07-20
    Organoaminosilanes, such as without limitation di-iso-propylaminosilane (DIPAS), are precursors for the deposition of silicon containing films such as silicon-oxide and silicon-nitride films. Described herein are methods to make organoaminosilane compounds, or other compounds such as organoaminodisilanes and organoaminocarbosilanes, via the catalytic hydrosilylation of an imine by a silicon source comprising a hydridosilane.
  • Organoaminosilane Precursors and Methods for Depositing Films Comprising Same
    申请人:Versum Materials US, LLC
    公开号:US20170207084A1
    公开(公告)日:2017-07-20
    Described herein are precursors and methods for forming silicon-containing films. In one aspect, the precursor comprises a compound represented by one of following Formulae A through E below: In one particular embodiment, the organoaminosilane precursors are effective for a low temperature (e.g., 350 ° C. or less), atomic layer deposition (ALD) or plasma enhanced atomic layer deposition (PEALD) of a silicon-containing film. In addition, described herein is a composition comprising an organoaminosilane described herein wherein the organoaminosilane is substantially free of at least one selected from the amines, halides (e.g., Cl, F, I, Br), higher molecular weight species, and trace metals.
  • Organoaminosilane Precursors And Methods For Depositing Films Comprising Same
    申请人:Versum Materials US, LLC
    公开号:US20200051811A1
    公开(公告)日:2020-02-13
    Described herein are precursors and methods for forming silicon-containing films. In one aspect, the precursor comprises a compound represented by one of following Formulae A through E below: In one particular embodiment, the organoaminosilane precursors are effective for a low temperature (e.g., 350° C. or less), atomic layer deposition (ALD) or plasma enhanced atomic layer deposition (PEALD) of a silicon-containing film. In addition, described herein is a composition comprising an organoaminosilane described herein wherein the organoaminosilane is substantially free of at least one selected from the amines, halides (e.g., Cl, F, I, Br), higher molecular weight species, and trace metals.
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同类化合物

甲磺酸 N,N-二甲基-2,2-二甲基乙烷次磺酰胺 2-甲基异噻唑烷 2-氰基-2-五氟苯基丁酸乙酯 N-methyl-N-tert.-octylthiomethylamine hydrochloride N-methyl-N-ethylthiomethylamine hydrochloride N-methyl-N-isopropylthiomethylamine hydrochloride perfluoro-2-methyl-1-cyclopenten-N,N-diethylsulfenamide 2-β-hydroxyethylthioethylamine hydrochloride 2-Amino-aethan-1-sulfensaeure N,N'-bis(1,1,1,2,3,3,3-heptafluoropropan-2-ylsulfanyl)-N,N'-dimethylethane-1,2-diamine N-[(1,1,2,2-Tetrachloroethyl)sulfanyl]methanamine 2-methyl-3,6-dihydro-1,2-thiazine N,N-dibutyl-hexane-1-sulfenamide N-[2-(dimethylaminosulfanyl)ethylsulfanyl]-N-methylmethanamine N-(butylthio)-tert-butylamine 1,1-dimethyl-ethanesulfenic acid dibutylamide N-Methylmethansulfenamid N-(tert-butylthio)ethylamine N-(tert-butylthio)butylamine N-(tert-butylthio)cyclohexylamine N,N-Dimethyl-2-chlortetrafluoraethansulfenamid N-<2-(Methlthio)-ethylthio>-dimethylamin N,N-Di-n-butylmethansulphenamid nonafluoro-n-butanesulfenic acid N-(Chlormethylthio)diethylamin N-[2-[2-[ethyl(methyl)amino]sulfanylethoxy]ethylsulfanyl]-N-methylethanamine N-ethyl-N-methyl-hexanesulfenamide N-(tert-butylthio)methylamine 2-isopropyl-4,5-dimethyl-3,6-dihydro-1,2-thiazine N-(Chlormethylthio)dimethylamin N-[1,1,1,3,3,3-hexafluoro-2-(trifluoromethyl)propan-2-yl]sulfanyl-N-methylmethanamine N-(Propan-2-yl)-N-(propylsulfanyl)propan-2-amine N-Ethyl-N-(propylsulfanyl)ethanamine N,N-dipropyl-propane-1-sulfenamide 2-methyl-N-(2-methylpropyl)-N-propylsulfanylpropan-1-amine N-Butylpropanesulfenamide N,N-diethylmethanesulfenamide 1-Chlor-N-(1,1,3,3-tetramethylbutyl)-1,1-bis(trifluormethyl)methansulfenamid N-(1-Adamantyl)-1-chlor-1,1-bis(trifluormethyl)methansulfenamid N-(tert-butylthio)isopropylamine 4-Propyl-1,3,4-oxathiazinane (5Z)-3-(methylsulfanylamino)-5-[(Z)-prop-1-enyl]nona-1,5-dien-2-olate N-ethyl-N-ethylsulfanyl-2-(methylideneamino)ethenamine 4,4-Dichloro-3-octylidene-1,2-thiazolidine N,2-dimethyl-N-methylsulfanylpentan-1-amine (1R,2R)-1,2-bis(hydroxysulfanyl)ethane-1,2-diol 2-(Methylaminosulfanyl)ethanamine 2-Ethyl-3-hydroxysulfanylbutan-1-ol 2-ethyl-2-methyl-N-(5-methylhexyl)-N-methylsulfanylhexan-1-amine