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p-Vinylphenyl-isocyanat | 2487-96-9

中文名称
——
中文别名
——
英文名称
p-Vinylphenyl-isocyanat
英文别名
1-Ethenyl-4-isocyanatobenzene
p-Vinylphenyl-isocyanat化学式
CAS
2487-96-9
化学式
C9H7NO
mdl
——
分子量
145.161
InChiKey
ZEIXNMVAJQLPMA-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:
    40.5-41.5 °C(Press: 0.1 Torr)
  • 密度:
    0.96±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.5
  • 重原子数:
    11
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    29.4
  • 氢给体数:
    0
  • 氢受体数:
    2

反应信息

  • 作为反应物:
    描述:
    p-Vinylphenyl-isocyanat 以91%的产率得到
    参考文献:
    名称:
    KORZHA I. D.; BARBA N. A.; SHUR A. M.; MANOLE S. F., BUL. AKAD. SHTIINTSE RSSMOLD., IZV. AN MOLDSSR. CEP. BIOL. I XIM. N. 1975+
    摘要:
    DOI:
  • 作为产物:
    描述:
    4-乙烯基苯甲酸 在 sodium azide 、 三乙胺 作用下, 以 丙酮甲苯 为溶剂, 反应 2.5h, 生成 p-Vinylphenyl-isocyanat
    参考文献:
    名称:
    A Novel Approach to the Molecular Imprinting of Polychlorinated Aromatic Compounds
    摘要:
    The aim of this investigation was to determine whether relatively weak interactions, such as hydrogen bonds to aromatic chlorine atoms and interactions involving aromatic pi electrons could be exploited within artificial receptors, constructed using the technique of molecular imprinting. For the purposes of this investigation we chose 2,3,7,8-tetrachlorodibenzodioxin (TCDD)as the model target. Imprinted polymers have been prepared with two new templates designed to create recognition sites for TCDD. The first of these, the bis-N-(4-vinylphenyl)urea derivative of 2,8-dichloro-3,7-diaminodibenzodioxin, employed a carbonyl spacer to introduce aromatic amines into the polymer after reductive cleavage of the template. The second, N-(2-(3,7,8-trichlorodibenzodioxinyl))-2-methacryloyloxybenzamide, incorporated a salicylic acid spacer and introduced a methacrylic acid residue into the polymer following hydrolysis. Both amine and acid groups were positioned in such a way as to interact with TCDD through the formation of weak hydrogen bonds to aromatic chlorine atoms. A second recognition element was introduced into the binding sites by the inclusion of a polymerizable, electron-rich, aromatic ether capable of forming pi-pi interactions with the electron-deficient dioxin molecule. Polymers imprinted with either template showed significantly higher uptake of TCDD than the corresponding nonimprinted controls, even at concentrations as low as 2 nM.
    DOI:
    10.1021/ja9818295
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文献信息

  • Amidate compound, catalyst for polyurethane production, and method for producing polyurethane resin
    申请人:KOEI CHEMICAL COMPANY, LIMITED
    公开号:US10689478B2
    公开(公告)日:2020-06-23
    Provided is an amidate compound represented by the formula (1): wherein A is a substituted or unsubstituted hydrocarbon group, n is an integer of 1 or more, and D is a nitrogen-containing organic group represented by the formula (2): wherein R1, R2, and R3 are the same or different, and are each a hydrocarbon group that may contain a heteroatom; some or all of R1, R2, and R3 may be bonded together to form a ring structure; X is a nitrogen atom, an oxygen atom, or a sulfur atom; and a is 0 or 1, wherein a is 1 when X is a nitrogen atom, and a is 0 when X is an oxygen atom or a sulfur atom.
    提供的是由式(1)表示的酰胺化合物:其中A是取代或未取代的碳氢基团,n是大于或等于1的整数,D是由式(2)表示的含氮有机基团:其中R1、R2和R3相同或不同,均为可能含有杂原子的碳氢基团;R1、R2和R3中的一些或全部可能结合在一起形成环结构;X是氮原子、氧原子或硫原子;a为0或1,当X为氮原子时,a为1,当X为氧原子或硫原子时,a为0。
  • Mechanochemical Release of <i>N</i> ‐Heterocyclic Carbenes from Flex‐Activated Mechanophores
    作者:Hang Shen、Michael B. Larsen、Allison G. Roessler、Paul M. Zimmerman、Andrew J. Boydston
    DOI:10.1002/anie.202100576
    日期:2021.6.7
    We have discovered a new flex-activated mechanophore that releases an N-heterocyclic carbene (NHC) under mechanical load. The mechanophore design is based upon NHC-carbodiimide (NHC-CDI) adducts and demonstrates an important first step toward flex-activated designs capable of further downstream reactivities. Since the flex-activation is non-destructive to the main polymer chains, the material can be
    我们发现了一种新的 flex-activated mechanophore,它在机械负载下释放 N-杂环卡宾 (NHC)。机械团设计基于 NHC-碳二亚胺 (NHC-CDI) 加合物,并展示了迈向能够进一步进行下游反应的柔性激活设计的重要第一步。由于弯曲激活对主聚合物链是非破坏性的,因此可以对材料进行多次压缩循环,以实现机械团激活百分比的迭代增加。展示了两种不同的 NHC 结构,表明机械设计的潜在模块化。
  • [EN] ADDITION-FRAGMENTATION OLIGOMERS<br/>[FR] OLIGOMÈRES D'ADDITION-FRAGMENTATION
    申请人:3M INNOVATIVE PROPERTIES CO
    公开号:WO2016133668A1
    公开(公告)日:2016-08-25
    Novel stress-reducing crosslinking oligomers that have application in dental restoratives, thin films, hardcoats, composites, adhesives, and other uses subject to stress reduction are described. The addition-fragmentation process of crosslinking results in a chain-transfer event that provides novel polymers that may be further functionalized. In addition, the addition-fragmentation oligomer comprises pendent functional groups that bond to a substrate by forming an ionic or covalent bond, or etch the substrate by chemically removing some material from the substrate.
    描述了一种在牙科修复、薄膜、硬涂层、复合材料、粘合剂等需要减压的用途中应用的新型减压交联寡聚体。交联的加成-断裂过程导致链转移事件,提供了可以进一步功能化的新型聚合物。此外,加成-断裂寡聚体包括侧链功能基团,通过形成离子键或共价键与基底结合,或通过化学去除基底上的部分材料来蚀刻基底。
  • Synthesis of polymeric 1-iminopyridinium ylides as photoreactive polymers
    作者:Daniel Klinger、Katja Nilles、Patrick Theato
    DOI:10.1002/pola.23832
    日期:2010.2.15
    by polymer analogous reactions on reactive precursor polymers. Quantitative conversion of the reactive groups was achieved with pentafluorophenyl ester containing polymers and newly synthesized photoreactive amines as well as by the reaction of poly(4‐vinylbenzoyl azide) with a photoreactive alcohol. The polymers obtained by both routes were examined regarding their photoreaction products and kinetics
    研究了聚合成1-亚氨基吡啶鎓碘化物作为新的光反应性聚合物结构的两种合成途径。在第一种方法中,通过自由基聚合实现了新合成的含1-亚氨基吡啶鎓叶立德的单体的聚合,生成了它们的聚合物类似物。或者,通过在反应性前体聚合物上进行聚合物类似反应,合成反应性前体聚合物并将其转化为相应的1-亚氨基吡啶鎓内鎓盐聚合物。含五氟苯基酯的聚合物和新合成的光反应性胺以及聚(4-乙烯基苯甲酰基叠氮化物)与光反应性醇的反应可实现反应基团的定量转化。检查通过这两种途径获得的聚合物的光反应产物和在溶液中以及在聚合物薄膜中的动力学。辐照前后聚合物膜上水的接触角测量结果表明,聚合物的亲水性发生了显着变化。©2010 Wiley Periodicals,Inc. J Polym Sci A部分:Polym Chem 48:832–844,2010年
  • [EN] PROCESS FOR PREPARING GUANIDINO-FUNCTIONAL MONOMERS<br/>[FR] PROCÉDÉ POUR LA PRÉPARATION DE MONOMÈRES À FONCTION GUANIDINO
    申请人:3M INNOVATIVE PROPERTIES CO
    公开号:WO2014204763A1
    公开(公告)日:2014-12-24
    A process for preparing guanidino-functional, free radically polymerizable compounds comprises (a) combining (1) an amine compound comprising (i) at least one primary aliphatic amino group and (ii) at least one secondary aliphatic amino group, primary aromatic amino group, or secondary aromatic amino group, and (2) a guanylating agent; (b) allowing or inducing reaction of the amine compound and the guanylating agent to form a guanylated amine compound; (c) combining (1) the guanylated amine compound, and (2) a reactive monomer comprising (i) at least one ethylenically unsaturated group and (ii) at least one group that is reactive with an amino group; and (d) allowing or inducing reaction of the guanylated amine compound and the reactive monomer to form a guanidino-functional, free radically polymerizable compound.
    制备胍基功能自由基聚合化合物的过程包括(a)结合(1)包含(i)至少一个主链脂肪氨基团和(ii)至少一个次级链脂肪氨基团、主链芳香胺基团或次级芳香胺基团的胺基化合物和(2)胍基化试剂;(b)允许或诱导胺基化合物和胍基化试剂发生反应以形成胍基化胺基化合物;(c)结合(1)胍基化胺基化合物和(2)包含(i)至少一个乙烯不饱和基团和(ii)至少一个与氨基反应的基团的反应单体;(d)允许或诱导胍基化胺基化合物和反应单体发生反应以形成胍基功能自由基聚合化合物。
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