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1,3-diisopropylimidazolium acetate | 1225462-87-2

中文名称
——
中文别名
——
英文名称
1,3-diisopropylimidazolium acetate
英文别名
1,3-Di(propan-2-yl)imidazol-1-ium;acetate;1,3-di(propan-2-yl)imidazol-1-ium;acetate
1,3-diisopropylimidazolium acetate化学式
CAS
1225462-87-2
化学式
C2H3O2*C9H17N2
mdl
——
分子量
212.292
InChiKey
IEYLUTXCTTXLPH-UHFFFAOYSA-M
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):
    0.69
  • 重原子数:
    15
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    48.9
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    聚合甲醛N,N'-二异丙基乙烷-1,2-二亚胺溶剂黄146 为溶剂, 反应 0.42h, 以78%的产率得到1,3-diisopropylimidazolium acetate
    参考文献:
    名称:
    易于获取的不对称不饱和2,6-二异丙基苯基N-杂环碳烯配体。在对映选择性催化中的应用
    摘要:
    一种新的多组分程序被用于合成(a)手性庞大的不对称不饱和2,6-二异丙基苯基N-杂环卡宾(NHC)前驱体,具有优异的选择性(高达95%)和良好的收率。这种方法提供了获得新的手性NHC配体的途径,这些配体已成功应用于铜催化的不对称烯丙基烷基化和铜催化的不对称硼化中。
    DOI:
    10.1021/acs.joc.6b02888
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文献信息

  • ISOCYANATE TRIMERISATION CATALYST SYSTEM, A PRECURSOR FORMULATION, A PROCESS FOR TRIMERISING ISOCYANATES, RIGID POLYISOCYANURATE/POLYURETHANE FOAMS MADE THEREFROM, AND A PROCESS FOR MAKING SUCH FOAMS
    申请人:Athey Phillip
    公开号:US20110201709A1
    公开(公告)日:2011-08-18
    The instant invention provides an isocyanate trimerisation catalyst system, a precursor formulation, a process for trimerising isocyanates, rigid foams made therefrom, and a process for making such foams. The trimerisation catalyst system comprises: (a) an imidazolium or imidazolinium cation; and (b) an isocyanate-trimer inducing anion; wherein said trimerisation catalyst system has a trimerisation activation temperature in the range of equal to or less than 73° C. The precursor formulation comprises: (1) at least 25 percent by weight of polyol, based on the weight of the precursor formulation; (2) less than 15 percent by weight of a trimerisation catalyst system, based on the weight of the precursor formulation, comprising; (a) an imidazolium or imidazolinium cation; and (c) an isocyanate-trimer inducing anion; wherein said trimerisation catalyst system has a trimerisation activation temperature in the range of equal to or less than 73° C.; and (3) optionally one or more surfactants, one or more flame retardants, water, one or more antioxidants, one or more auxiliary blowing agents, one or more urethane catalysts, one or more auxiliary trimerisation catalysts, or combinations thereof. The process for trimerisation of isocyanates comprises the steps of: (1) providing one or more monomers selected from the group consisting of an isocyanate, a diisocyanate, a triisocyanatetriisocyanate, oligomeric isocyanate, a salt of any thereof, and a mixture of any thereof; (2) providing a trimerisation catalyst system comprising; (a) an imidazolium or imidazolinium cation; and (b) an isocyanate-trimer inducing anion; (c) wherein said trimerisation catalyst system has a trimerisation activation temperature in the range of equal to or less than 73° C.; (3) trimerising said one or more monomers in the presence of said trimerisation catalyst; (4) thereby forming an isocyanurate trimer. The process for making the PIR foam comprises the steps of: (1) providing one or more monomers selected from the group consisting of an isocyanate, a diisocyanate, a triisocyanatetriisocyanate, oligomeric isocyanate, a salt of any thereof, and a mixture any thereof; (2) providing polyol; (3) providing a trimerisation catalyst system comprising; (a) an imidazolium or imidazolinium cation; and (b) an isocyanate-timer inducing anion; wherein said trimerisation catalyst system has a trimerisation activation temperature in the range of equal to or less than 73° C.; and (4) optionally providing one or more surfactants, one or more flame retardants, water, one or more antioxidants, one or more auxiliary blowing agents, one or more urethane catalysts, one or more auxiliary trimerisation catalysts, or combinations thereof; (5) contacting said one or more monomers, and said polyol, and optionally said one or more surfactants, and optionally said one or more flame retardants, and optionally said water, and optionally said one or more antioxidants, and optionally said one or more auxiliary blowing agents in the presence of said trimerisation catalyst system and optionally said one or more urethane catalysts, and optionally said one or more auxiliary trimerisation catalysts; (6) thereby forming said polyisocyanurate/polyurethane rigid foam. The PIR foam comprises the reaction product of one or more monomers selected from the group consisting of an isocyanate, a diisocyanate, a triisocyanatetriisocyanate, oligomeric isocyanate, a salt of any thereof, and a mixture any thereof with polyol in the presence of a trimerisation catalyst system comprising an imidazolium or imidazolinium cation, and an isocyanate-trimer inducing anion, and optionally one or more surfactants, optionally one or more flame retardants, optionally water, optionally one or more antioxidants, optionally one or more auxiliary blowing agents, optionally one or more additional urethane catalysts, and optionally one or more auxiliary trimerisation catalysts, or optionally combinations thereof, wherein the trimerisation catalyst system has a trimerisation activation temperature in the range of equal to or less than 73° C. The PIR foam comprises the reaction product of one or more monomers selected from the group consisting of an isocyanate, a diisocyanate, a triisocyanatetriisocyanate, oligomeric isocyanate, a salt of any thereof, and a mixture any thereof with polyol in the presence of a trimerisation catalyst system comprising an imidazolium or imidazolinium cation, and an isocyanate-trimer inducing anion, and optionally one or more surfactants, optionally one or more flame retardants, optionally water, optionally one or more antioxidants, optionally one or more auxiliary blowing agents, optionally one or more additional polyurethane catalysts, and optionally one or more auxiliary trimerisation catalysts, or optionally combinations thereof, wherein the PIR foam has a polyisocyanurate trimer ratio (Abs 1410 /Abs 1595 ) of at least 5 at a depth of 12 mm from the rising surface of the rigid foam, measured via ATR-FTIR spectroscopy.
    该发明提供了一种异氰酸酯三聚催化剂系统、前体配方、异氰酸酯三聚化过程、由此制成的硬质泡沫以及制备此类泡沫的方法。该三聚化催化剂系统包括:(a)咪唑或咪唑啉阳离子;以及(b)异氰酸酯三聚诱导阴离子;其中所述的三聚化催化剂系统具有等于或小于73℃的三聚化活化温度。前体配方包括:(1)聚醚醇,其重量占前体配方重量的至少25%;(2)三聚化催化剂系统,其重量占前体配方重量的15%以下,包括:(a)咪唑或咪唑啉阳离子;(b)异氰酸酯三聚诱导阴离子;其中所述的三聚化催化剂系统具有等于或小于73℃的三聚化活化温度;以及(3)可选的一个或多个表面活性剂、一个或多个阻燃剂、水、一个或多个抗氧化剂、一个或多个辅助发泡剂、一个或多个脲催化剂、一个或多个辅助三聚化催化剂或其组合。异氰酸酯三聚化过程包括以下步骤:(1)提供一种或多种单体,所述单体选自群组中的异氰酸酯、二异氰酸酯、三异氰酸酯三异氰酸酯、寡聚异氰酸酯、任何其中的盐以及任何其中的混合物;(2)提供三聚化催化剂系统,包括:(a)咪唑或咪唑啉阳离子;以及(b)异氰酸酯三聚诱导阴离子;其中所述的三聚化催化剂系统具有等于或小于73℃的三聚化活化温度;(3)在所述三聚化催化剂的存在下,三聚化所述的一种或多种单体;(4)从而形成异氰酸酯三聚体。制备PIR泡沫的方法包括以下步骤:(1)提供一种或多种单体,所述单体选自群组中的异氰酸酯、二异氰酸酯、三异氰酸酯三异氰酸酯、寡聚异氰酸酯、任何其中的盐以及任何其中的混合物;(2)提供聚醚醇;(3)提供三聚化催化剂系统,包括:(a)咪唑或咪唑啉阳离子;以及(b)异氰酸酯三聚诱导阴离子;其中所述的三聚化催化剂系统具有等于或小于73℃的三聚化活化温度;以及(4)可选地提供一个或多个表面活性剂、一个或多个阻燃剂、水、一个或多个抗氧化剂、一个或多个辅助发泡剂、一个或多个脲催化剂、一个或多个辅助三聚化催化剂或其组合;(5)在所述三聚化催化剂系统和可选的一个或多个脲催化剂以及可选的一个或多个辅助三聚化催化剂的存在下,将所述的一种或多种单体、所述的聚醚醇、可选的一个或多个表面活性剂、可选的一个或多个阻燃剂、可选的水、可选的一个或多个抗氧化剂以及可选的一个或多个辅助发泡剂接触;(6)从而形成所述的聚异氰酸酯/聚氨酯硬质泡沫。PIR泡沫是由异氰酸酯、二异氰酸酯、三异氰酸酯三异氰酸酯、寡聚异氰酸酯、任何其中的盐以及任何其中的混合物和聚醚醇在咪唑或咪唑啉阳离子和异氰酸酯三聚诱导阴离子以及可选的一个或多个表面活性剂、可选的一个或多个阻燃剂、可选的水、可选的一个或多个抗氧化剂、可选的一个或多个辅助发泡剂、可选的一个或多个额外脲催化剂以及可选的一个或多个辅助三聚化催化剂或其组合的存在下的反应产物,其中所述的三聚化催化剂系统具有等于或小于73℃的三聚化活化温度。PIR泡沫在距硬质泡沫上升表面12mm处通过ATR-FTIR光谱测量具有聚异氰酸酯三聚体比值(Abs1410/Abs1595)至少为5。
  • CATALYSTS FOR POLYURETHANE COATING COMPOUNDS
    申请人:Neu Oliver
    公开号:US20120288632A1
    公开(公告)日:2012-11-15
    The present invention relates to coating compositions for polyurethane coating materials that feature new catalysts.
    本发明涉及用于聚氨酯涂层材料的涂料组合物,其具有新的催化剂。
  • PROCESS FOR THE PREPARATION OF CHALCOGENE COMPOUNDS
    申请人:Petroliam Nasional Berhad (PETRONAS)
    公开号:EP2417109B1
    公开(公告)日:2014-12-03
  • KATALYSATOREN FÜR POLYURETHANBESCHICHTUNGSMASSEN
    申请人:BASF SE
    公开号:EP2504372B1
    公开(公告)日:2015-01-07
  • Process For The Preparation Of Chalcogene Compounds
    申请人:Rogers Robin Don
    公开号:US20120108822A1
    公开(公告)日:2012-05-03
    The present invention is a novel process for the preparation of chalcogenone compounds by conversion of ionic liquids and salts comprising nitrogen-containing heterocyclic cations and basic anions to the corresponding nitrogen-containing heterocyclic chalcogenones by reaction with elemental chalcogens.
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同类化合物

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