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3-甲基戊-4-烯酰胺 | 87168-54-5

中文名称
3-甲基戊-4-烯酰胺
中文别名
——
英文名称
3-methylpent-4-enoic acid amide
英文别名
3-methylpent-4-enylcarboxamide;3-methyl-4-pentenamide;3-methylpent-4-enamide
3-甲基戊-4-烯酰胺化学式
CAS
87168-54-5
化学式
C6H11NO
mdl
MFCD19203686
分子量
113.159
InChiKey
GIRDSTDJQGAWQD-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:
    228.1±19.0 °C(Predicted)
  • 密度:
    0.913±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.5
  • 重原子数:
    8
  • 可旋转键数:
    3
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    43.1
  • 氢给体数:
    1
  • 氢受体数:
    1

SDS

SDS:aeb02722333f0cfd65ca3cb23e488a06
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    3-甲基戊-4-烯酰胺 在 lithium aluminium tetrahydride 作用下, 以 四氢呋喃 为溶剂, 生成 3-methylpent-4-enylamine
    参考文献:
    名称:
    的立体选择性合成Ñ通过γ-的Pd-催化的反应( -保护的吡咯烷ñ -酰基)烯烃和γ-(Ñ -Boc -氨基)链烯与芳基溴化物
    摘要:
    描述了通过Pd催化的γ-(N-酰基氨基)烯烃和γ-(N -Boc-氨基)烯烃与芳基溴的立体反应合成的N-酰基和N - Boc保护的吡咯烷。这些反应在一次操作中实现两个键的形成,并且通常以高水平的非对映选择性进行。与先前描述的γ-(N-芳基氨基)烯烃反应相反,这些转化反应在富电子和缺电子的芳基溴化物以及乙烯基溴化物底物下均以高收率和高区域选择性进行。
    DOI:
    10.1016/j.tet.2005.03.110
  • 作为产物:
    描述:
    chloro-[(3-methyl-5-oxopyrrolidin-2-yl)methyl]mercury 在 sodium trimethoxyborohydride 作用下, 以100%的产率得到3-甲基戊-4-烯酰胺
    参考文献:
    名称:
    Efficient Coupling reactions of β-Amino and β-Acetamido Radicals with Electron Deficient Alkenes - Aza-Carbofunctionalization of Olefins - A Promising New Tool for Alkaloid Synthesis.
    摘要:
    DOI:
    10.1016/s0040-4039(00)81841-9
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文献信息

  • Expedient Pathway into Optically Active 2-Oxopiperidines
    作者:Sebastiaan Bas A. M. W. van den Broek、Peter G. W. Rensen、Floris L. van Delft、Floris P. J. T. Rutjes
    DOI:10.1002/ejoc.201000587
    日期:2010.10
    The piperidine ring system is one of the most common structural subunits and is found in many natural products. Moreover, piperidine alkaloids and derivatives thereof are of great interest for the pharmaceutical industry since they exhibit a wide range of biological activities. Consequently, short and valuable routes to highly functionalized building blocks for this important ring system are of general
    哌啶环系统是最常见的结构亚基之一,存在于许多天然产物中。此外,哌啶生物碱及其衍生物在制药工业中具有重要意义,因为它们表现出广泛的生物活性。因此,人们普遍感兴趣的是,为这个重要的环系统提供高度功能化的构建模块的简短而有价值的途径。开发了一种基于线性(取代)脱氢氨基酯的闭环复分解 (RCM) 介导的方法来提供环状脱氢氨基酯。这些结构代表了通往高度取代的哌啶酸以及更复杂的杂环的有价值的中间体。
  • Stereoselective Selenolactonization by Superelectrophilic Benzeneselenenyl Triflate
    作者:Shizuaki Murata、Toshiyasu Suzuki
    DOI:10.1246/cl.1987.849
    日期:1987.5.5
    Benzeneselenenyl triflate is prepared from benzeneselenenyl chloride and silver trifluoromethanesulfonate. It performs selenium-induced cyclization of β,γ-, γ,δ-, and δ,ε-unsaturated carboxylic acids.
    苯硒三氟甲磺酸酯是由苯硒氯化物和三氟甲磺酸银制备的。它能够促进β,γ-、γ,δ-和δ,ε-不饱和羧酸的硒诱导环化反应。
  • Stereoselective synthesis of N-protected pyrrolidines via Pd-catalyzed reactions of γ-(N-acylamino) alkenes and γ-(N-Boc-amino) alkenes with aryl bromides
    作者:Myra Beaudoin Bertrand、John P. Wolfe
    DOI:10.1016/j.tet.2005.03.110
    日期:2005.6
    stereoselective synthesis of N-acyl- and N-Boc-protected pyrrolidines via Pd-catalyzed reactions of γ-(N-acylamino) alkenes and γ-(N-Boc-amino) alkenes with aryl bromides is described. These reactions effect formation of two bonds in a single operation and proceed with generally high levels of diastereoselectivity. In contrast to previously described reactions of γ-(N-arylamino) alkenes, these transformations
    描述了通过Pd催化的γ-(N-酰基氨基)烯烃和γ-(N -Boc-氨基)烯烃与芳基溴的立体反应合成的N-酰基和N - Boc保护的吡咯烷。这些反应在一次操作中实现两个键的形成,并且通常以高水平的非对映选择性进行。与先前描述的γ-(N-芳基氨基)烯烃反应相反,这些转化反应在富电子和缺电子的芳基溴化物以及乙烯基溴化物底物下均以高收率和高区域选择性进行。
  • Molecular Healing of Polymeric Materials, Coatings, Plastics, Elastomers, Composites, Laminates, Adhesives, and Sealants by Active Enzymes
    申请人:McDaniel C. Steven
    公开号:US20100210745A1
    公开(公告)日:2010-08-19
    Disclosed herein are polymeric materials such as a coating, a plastic, a laminate, a composite, an elastomer, an adhesive, or a sealant; a surface treatment such as a textile finish or a wax; a filler for such a polymeric material or a surface treatment that includes an enzyme such as an esterase (e.g., a lipolytic enzyme, a sulfuric ester hydrolase, an organophosphorus compound degradation enzyme), an enzyme (e.g., a lysozyme, a lytic transglycosylase) that degrades a cell wall and/or a cell membrane component, a biocidal or biostatic peotide, and/or a peptidase. Also disclosed herein are methods of altering a material's property such as service life, flexability, or rigidity, by incorporation of an enzyme into a material capable of being chemically crosslinked by the activity of a lipolytic enzyme, a hydrolase, and/or a urease.
    本文公开了一些聚合材料,如涂层、塑料、层压板、复合材料、弹性体、粘合剂或密封剂;一种表面处理,如纺织品涂层或蜡;一种填料,用于这样的聚合材料或表面处理,其中包括一种酶,如酯酶(例如,脂肪水解酶,硫酸酯水解酶,有机磷化合物降解酶),降解细胞壁和/或细胞膜成分的酶(例如,溶菌酶,裂解转糖基酶),生物杀菌或生物静态肽,以及/或肽酶。本文还公开了通过将酶纳入可通过脂肪水解酶、水解酶和/或脲酶的活性交联材料中来改变材料性能,如使用寿命、柔韧性或刚度的方法。
  • Polymeric Coatings Incorporating Bioactive Enzymes for Catalytic Function
    申请人:McDaniel C. Steven
    公开号:US20120097194A1
    公开(公告)日:2012-04-26
    Disclosed herein are materials including a polymeric materials such as a coating, a plastic, a laminate, a composite, an elastomer, an adhesive, or a sealant; a surface treatment such as a coating, a textile finish or a wax; a filler for such a polymeric material or a surface treatment, which includes an enzyme such as an esterase (e.g., a lipolytic enzyme, an organophosphorus compound degradation enzyme), wherein the enzyme decontaminates a chemical from the surface of the material. Also disclosed herein are methods of cleaning a surface of a material that comprises an enzyme.
    本文公开了一种材料,包括聚合物材料,例如涂层、塑料、层压板、复合材料、弹性体、粘合剂或密封剂;表面处理,例如涂层、纺织品处理或蜡;用于上述聚合物材料或表面处理的填料,其中包括酶,例如酯酶(例如脂肪水解酶、有机磷化合物降解酶),其中酶可从材料表面去除化学物质。本文还公开了一种清洁含有酶的材料表面的方法。
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