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4-isopropyl-m-phenylene diisocyanate | 17022-08-1

中文名称
——
中文别名
——
英文名称
4-isopropyl-m-phenylene diisocyanate
英文别名
4-Isopropyl-m-phenylendiisocyanat;cumene 2,4-diisocyanate;2,4-Diisocyanato-1-propan-2-ylbenzene
4-isopropyl-<i>m</i>-phenylene diisocyanate化学式
CAS
17022-08-1
化学式
C11H10N2O2
mdl
——
分子量
202.213
InChiKey
VXQILLTWRZPRQF-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):
    4.6
  • 重原子数:
    15
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    58.9
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

点击查看最新优质反应信息

文献信息

  • Release sustaining composition and sustained release preparation
    申请人:Hayakawa Kazuhisa
    公开号:US20050147676A1
    公开(公告)日:2005-07-07
    A release sustaining composition comprising a polyalkylene polyol derivative comprising repeating units U-1 derived from a water-soluble polyalkylene polyol and a polyisocyanate and repeating units U-2 derived from a dihydroxy compound and a polyisocyanate in a molar ratio of U-1/U-2 between 0.5/0.5 and 0.99/0.01 and optionally a water-soluble cellulose ether is combined with an active ingredient to make a sustained release preparation.
    一种持续释放组合物,包括由可溶于水的聚烯烃聚醚和聚异氰酸酯衍生的重复单元U-1以及由二羟基化合物和聚异氰酸酯衍生的重复单元U-2,在U-1/U-2的摩尔比在0.5/0.5至0.99/0.01之间,可选地与可溶于水的纤维素醚结合,用于制备持续释放制剂。
  • 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。
  • D1479 STABLE LIQUID BAP PHOTOINITIATOR AND ITS USE IN RADIATION CURABLE COMPOSITIONS
    申请人:DSM IP ASSETS B.V.
    公开号:US20130237626A1
    公开(公告)日:2013-09-12
    The invention relates to radiation curable compositions comprising a liquid 0/s(acyl)phosphine photo initiators of formula (I): wherein each of Ar 1 , Ar 2 and Ar 3 is independently a substituted or unsubstituted aryl group. The invention also relates to stabilized forms of liquid bis(acyl)phosphines of formula (I) and radiation curable composition comprising said stabilized photoinitiators. The radiation curable compositions are selected from the group consisting of an optical fiber coating composition and a coating composition capable of radiation cure on concrete and a coating composition capable of radiation cure on metal.
    本发明涉及一种辐射可固化组合物,其包括液体0/s(酰基)膦光引发剂,其化学式为(I):其中Ar1、Ar2和Ar3中的每一个独立地是取代或未取代的芳基基团。本发明还涉及化学式(I)的液态双(酰基)膦的稳定形式和包括所述稳定光引发剂的辐射可固化组合物。所述辐射可固化组合物选自光纤涂层组合物、能够在混凝土上辐射固化的涂层组合物和能够在金属上辐射固化的涂层组合物。
  • SIZING AGENT FOR CARBON FIBER, CARBON FIBER WITH IMPROVED INTERFACIAL ADHESION, POLYMERIZATION REACTION TYPE CARBON FIBER-REINFORCED POLYMER COMPOSITE MATERIAL USING SAME, AND PRODUCTION METHOD THEREFOR
    申请人:KOREA INSTITUTE OF MACHINERY & MATERIALS
    公开号:US20190284751A1
    公开(公告)日:2019-09-19
    The present invention relates to a sizing agent for carbon fibers, a carbon fiber with improved interfacial adhesion, a polymerization reaction type carbon fiber-reinforced polymer composite material using the same, and a production method therefor and, more specifically, to a sizing agent for carbon fibers, comprising a phenoxy resin and a block isocyanate compound prepared through a reaction of ε-caprolactam with one of two isocyanate groups of a diisocyanate compound, and the production of a carbon fiber with improved interfacial adhesion using the same, a polymerization reaction type carbon fiber-reinforced polymer composite material using the carbon fiber with improved interfacial adhesion, and a production method therefor.
    本发明涉及一种用于碳纤维的分散剂、改善界面黏附的碳纤维、采用该分散剂制备的聚合反应型碳纤维增强聚合物复合材料以及其生产方法,更具体地,涉及一种用于碳纤维的分散剂,包括一种苯氧树脂和一种经由ε-己内酰胺与二异氰酸酯化合物的两个异氰酸基中的一个反应制备的块状异氰酸酯化合物,并使用该分散剂生产改善界面黏附的碳纤维,采用改善界面黏附的碳纤维制备的聚合反应型碳纤维增强聚合物复合材料,以及其生产方法。
  • Non-fugitive diaminobenzoate catalytic chain extenders
    申请人:AIR PRODUCTS AND CHEMICALS, INC.
    公开号:EP0300349A1
    公开(公告)日:1989-01-25
    The present invention relates a process for the production of polyurethanes wherein a tertiary amine functionality is incorporated into the side chain of a diaminobenzoate, to form a non-fugitive catalyst polyurethane chain extender. These non-fugitive chain extenders are polyurethane catalysts that provide adequate cure without residual odor and safety hazards associated with the more traditional tertiary amine catalysts. When reacted with the isocyanate reactive group the non-tertiary amine portion of the chain extender is bound to the polymeric network. Diffusion of the catalyst species from the polyurethane has been prevented, thus negating odor and toxicity as a problem. The diaminobenzoate provides enhanced polyurethane physical properties.
    本发明涉及一种生产聚氨酯的方法,其中将三级胺功能并入二氨基苯甲酸酯的侧链中,形成一种非挥发催化剂聚氨酯链延伸剂。这些非挥发性链延伸剂是聚氨酯催化剂,可提供足够的固化,而不会产生与传统三级胺催化剂相关的残留气味和安全隐患。当与异氰酸酯反应的反应基团结合后,链延伸剂的非三级胺部分被结合到聚合物网络中。防止了催化剂物种从聚氨酯中扩散,从而消除了气味和毒性问题。二氨基苯甲酸酯提供了增强的聚氨酯物理性能。
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