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2,2-二乙基丙二腈 | 28118-33-4

中文名称
2,2-二乙基丙二腈
中文别名
——
英文名称
2,2-diethyl-malononitrile
英文别名
Diethylmalonsaeuredinitril;diethyl malononitrile;2,2-Diethylmalononitrile;2,2-diethylpropanedinitrile
2,2-二乙基丙二腈化学式
CAS
28118-33-4
化学式
C7H10N2
mdl
MFCD01570048
分子量
122.17
InChiKey
AIEHSKCCVPIDNR-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

  • 熔点:
    44 °C
  • 沸点:
    53 °C(Press: 5 Torr)
  • 密度:
    0.933±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.5
  • 重原子数:
    9
  • 可旋转键数:
    2
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.714
  • 拓扑面积:
    47.6
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:3438da3cedb9037cf68961ffff86254d
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反应信息

  • 作为反应物:
    描述:
    2,2-二乙基丙二腈 在 lithium aluminium tetrahydride 作用下, 以 乙醚 为溶剂, 生成 2,2-二乙基丙烷-1,3-二胺
    参考文献:
    名称:
    外消旋丙交酯的立体选择性开环聚合反应,通过使用非手性salen-和sasalen-铝复合物进行。
    摘要:
    高度全同立构的聚丙交酯或聚乳酸在外消旋丙交酯的开环聚合(ROP)中与非手性salen-和高salen-铝配合物(salenH(2)= N,N'-双(水杨基)乙烯-1)合成,2-二胺;高沙仑H(2)= N,N′-双(水杨基)三亚甲基-1,3-二胺)。对配体的系统研究表明,席夫碱部分对等规度和高活性骨架的立体影响很重要。原位制备的配合物足够纯,无需纯化即可用于聚合反应。通过X射线衍射阐明了关键配合物的晶体结构,这证实了它们是手性的。然而,(1)H和(13)C NMR谱的分析清楚地表明,它们的构象是如此灵活,以致于在25℃下不能将络合物的手性环境维持在溶液中,并且该络合物在聚合条件下是非手性的。还记录了骨干在传播步骤中的灵活性。因此,聚合物的全同立构规整度由于链端控制机理而发生。本系统中的最高反应性是通过在骨架上具有2,2-二甲基取代基的高均烯配体(ArCH == NCH(2)CMe(2)CH(2)N
    DOI:
    10.1002/chem.200601308
  • 作为产物:
    参考文献:
    名称:
    THE REACTION BETWEEN BARBITAL (DIETHYLBARBITURIC ACID) AND PHOSPHORUS PENTACHLORIDE
    摘要:
    DOI:
    10.1021/ja01355a059
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文献信息

  • THIOPHENE END GROUPS OF NON-FULLERENE ACCEPTORS FOR ELECTRONIC AND PHOTONIC APPLICATIONS
    申请人:The Hong Kong University of Science and Technology
    公开号:US20200347077A1
    公开(公告)日:2020-11-05
    Provided herein are small molecular acceptor compounds containing thiophene end groups, methods for their preparation and intermediates used therein, the use of formulations containing the same as semiconductors in organic electronic devices, especially in organic photovoltaic and organic field-effect transistor devices, and to organic electronic and organic photovoltaic devices made from these formulations.
    本文提供了含有噻吩末端基团的小分子受体化合物,其制备方法及其中使用的中间体,以及包含这些化合物的配方在有机电子器件中作为半导体的用途,特别是在有机光伏和有机场效应晶体管器件中的应用,以及由这些配方制成的有机电子和有机光伏器件。
  • CHEMICAL MECHANICAL POLISHING AND WAFER CLEANING COMPOSITION COMPRISING AMIDOXIME COMPOUNDS AND ASSOCIATED METHOD FOR USE
    申请人:Lee Wai Mun
    公开号:US20090130849A1
    公开(公告)日:2009-05-21
    A composition and associated method for chemical mechanical planarization (or other polishing) is described. The composition contains an amidoxime compound and water. The composition may also contain an abrasive and a compound with oxidation and reduction potential. The composition is useful for attaining improved removal rates for metal, including copper, barrier material, and dielectric layer materials in metal CMP. The composition is particularly useful in conjunction with the associated method for metal CMP applications.
    本文描述了一种化学机械平整化(或其他抛光)的组合物及其相关方法。该组合物含有一种酰胺肟化合物和水。该组合物还可以含有磨料和具有氧化还原潜力的化合物。该组合物可用于在金属CMP中获得改进的金属去除速率,包括铜、屏障材料和金属CMP中的介电层材料。该组合物在金属CMP应用的相关方法中特别有用。
  • METHODS OF CLEANING SEMICONDUCTOR DEVICES AT THE BACK END OF LINE USING AMIDOXIME COMOSITIONS
    申请人:Lee Wai Mun
    公开号:US20100043823A1
    公开(公告)日:2010-02-25
    The present invention relates to aqueous compositions comprising amidoxime compounds and methods for cleaning plasma etch residue from semiconductor substrates including such dilute aqueous solutions. The compositions of the invention may optionally contain one or more other acid compounds, one or more basic compounds, and a fluoride-containing compound and additional components such as organic solvents, chelating agents, amines, and surfactants. The invention also relates to a method of removing residue from a substrate during integrated circuit fabrication.
    本发明涉及含有酰胺肟化合物的水性组合物及其清洗半导体衬底上等离子体刻蚀残留物的方法,包括这种稀释的水性溶液。本发明的组合物可以选择性地含有一种或多种其他酸性化合物、一种或多种碱性化合物、含氟化合物和其他成分,如有机溶剂、螯合剂、胺和表面活性剂。本发明还涉及一种在集成电路制造过程中从衬底上去除残留物的方法。
  • SULFONYLPYRAZOLE AND SULFONYLPYRAZOLINE CARBOXAMIDINE DERIVATIVES AS 5-HT6 ANTAGONISTS
    申请人:Van Loevezijn Arnold
    公开号:US20080311179A1
    公开(公告)日:2008-12-18
    This invention concerns compounds of the general formula (1). and derivatives thereof, which are antagonists of 5-HT 6 receptors, wherein the symbols have the meanings given in the description. The invention also concerns methods for the preparation of these compounds, to novel intermediates useful for their synthesis, and to uses of such compounds and compositions, particularly their use in administering them to patients to achieve a therapeutic effect in treating at least on disease or condition chosen from Parkinson's disease, Huntington's chorea, schizophrenia, anxiety, depression, manic depression, psychoses, epilepsy, obsessive compulsive disorders, mood disorders, migraine, Alzheimer's disease, age related cognitive decline, mild cognitive impairment, sleep disorders, eating disorders, anorexia, bulimia, binge eating disorders, panic attacks, akathisia, attention deficit hyperactivity disorder, attention deficit disorder, withdrawal from abuse of cocaine, ethanol, nicotine or benzodiazepines, pain, disorders associated with spinal trauma or head injury, hydrocephalus, functional bowel disorder, Irritable Bowel Syndrome, obesity and type-2 diabetes.
    本发明涉及通式(1)的化合物及其衍生物,它们是5-HT6受体拮抗剂,其中符号的含义如说明书所示。本发明还涉及制备这些化合物的方法,对于其合成有用的新型中间体,以及这些化合物和组合物的用途,特别是将它们用于向患者施用以达到治疗帕金森病、亨廷顿舞蹈症、精神分裂症、焦虑、抑郁症、躁郁症、精神病、癫痫、强迫症、情绪障碍、偏头痛、阿尔茨海默病、与年龄相关的认知衰退、轻度认知障碍、睡眠障碍、进食障碍、厌食症、贪食症、暴食症、惊恐发作、不安定症、注意力缺陷多动障碍、注意力缺陷障碍、戒断可卡因、乙醇、尼古丁或苯二氮平的滥用、疼痛、与脊髓损伤或头部损伤有关的疾病、脑积水、功能性肠道障碍、肠易激综合征、肥胖症和2型糖尿病等至少一种疾病或症状的治疗效果。
  • Sulfonylpyrazole and sulfonylpyrazoline carboxamidine derivatives as 5-HT6 antagonists
    申请人:Solvay Pharmaceuticals B.V.
    公开号:US07728018B2
    公开(公告)日:2010-06-01
    This invention concerns compounds of the general formula (1): and derivatives thereof, which are antagonists of 5-HT6 receptors, wherein the symbols have the meanings given in the description. The invention also concerns methods for the preparation of these compounds, to novel intermediates useful for their synthesis, and to uses of such compounds and compositions, particularly their use in administering them to patients to achieve a therapeutic effect in treating at least on disease or condition chosen from Parkinson's disease, Huntington's chorea, schizophrenia, anxiety, depression, manic depression, psychoses, epilepsy, obsessive compulsive disorders, mood disorders, migraine, Alzheimer's disease, age related cognitive decline, mild cognitive impairment, sleep disorders, eating disorders, anorexia, bulimia, binge eating disorders, panic attacks, akathisia, attention deficit hyperactivity disorder, attention deficit disorder, withdrawal from abuse of cocaine, ethanol, nicotine or benzodiazepines, pain, disorders associated with spinal trauma or head injury, hydrocephalus, functional bowel disorder, Irritable Bowel Syndrome, obesity and type-2 diabetes.
    这项发明涉及一般式(1)的化合物及其衍生物,它们是5-HT6受体的拮抗剂,其中符号具有描述中所给出的含义。该发明还涉及制备这些化合物的方法,对于其合成有用的新中间体,以及这些化合物和组合物的用途,特别是将它们用于给患者治疗至少一种疾病或病状,包括帕金森病、亨廷顿舞蹈症、精神分裂症、焦虑症、抑郁症、躁郁症、精神病、癫痫、强迫症、情绪障碍、偏头痛、阿尔茨海默病、与年龄相关的认知衰退、轻度认知障碍、睡眠障碍、进食障碍、厌食症、贪食症、暴食症、惊恐发作、不安躁动、注意力缺陷多动障碍、注意力缺陷障碍、戒断可卡因、乙醇、尼古丁或苯二氮平的滥用、疼痛、与脊髓损伤或头部损伤相关的疾病、脑积水、功能性肠道紊乱、肠易激综合征、肥胖症和2型糖尿病。
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同类化合物

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