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Diisopropylamino ethyl sulfide | 134441-13-7

中文名称
——
中文别名
——
英文名称
Diisopropylamino ethyl sulfide
英文别名
N-ethylsulfanyl-N-propan-2-ylpropan-2-amine
Diisopropylamino ethyl sulfide化学式
CAS
134441-13-7
化学式
C8H19NS
mdl
——
分子量
161.312
InChiKey
AUHZRDQYASNPPC-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

物化性质

  • 沸点:
    196.4±23.0 °C(Predicted)
  • 密度:
    0.883±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.7
  • 重原子数:
    10
  • 可旋转键数:
    4
  • 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:
    参考文献:
    名称:
    关于异戊二烯的直​​接金属化
    摘要:
    异戊二烯已在四氢呋喃中与过量的空间受阻的二烷基酰胺化钾金属化,这是通过等摩尔量的相应的氨基化锂和叔丁醇钾的混合制备的。随后与环氧乙烷,烷基溴化物和苯乙醛的反应以合理的收率得到了预期的偶联产物。与(CH 3)2 CHCH 2 CH = O和(CH 3)2 C =CHCH =O偶合,以低收率得到树皮甲虫信息素(±)-异酚和(±)-异戊二烯酚。
    DOI:
    10.1016/s0040-4020(01)96114-9
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文献信息

  • US6599733B1
    申请人:——
    公开号:US6599733B1
    公开(公告)日:2003-07-29
  • US7001758B1
    申请人:——
    公开号:US7001758B1
    公开(公告)日:2006-02-21
  • On the direct metalation of isoprene
    作者:P.A.A. Klusener、L. Tip、L. Brandsma
    DOI:10.1016/s0040-4020(01)96114-9
    日期:1991.3
    Isoprene has been metalated in tetrahydrofuran with an excess of sterically hindered potassium dialkylamides, prepared by combining equimolar amounts of the corresponding lithium amide and potassium tert-butoxide. Subsequent reaction with oxirane, alkyl bromides, and pivaldehyde gave the expected coupling products in reasonable yields. Coupling with (CH3)2CHCH2CHO and (CH3)2CCHCHO afforded the bark
    异戊二烯已在四氢呋喃中与过量的空间受阻的二烷基酰胺化钾金属化,这是通过等摩尔量的相应的氨基化锂和叔丁醇钾的混合制备的。随后与环氧乙烷,烷基溴化物和苯乙醛的反应以合理的收率得到了预期的偶联产物。与(CH 3)2 CHCH 2 CH = O和(CH 3)2 C =CHCH =O偶合,以低收率得到树皮甲虫信息素(±)-异酚和(±)-异戊二烯酚。
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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