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Prop-2-ynyl 3-[3-[2,2-bis[3-(3-oxo-3-prop-2-ynoxypropyl)sulfanylpropanoyloxymethyl]butoxy]-3-oxopropyl]sulfanylpropanoate | 1224867-84-8

中文名称
——
中文别名
——
英文名称
Prop-2-ynyl 3-[3-[2,2-bis[3-(3-oxo-3-prop-2-ynoxypropyl)sulfanylpropanoyloxymethyl]butoxy]-3-oxopropyl]sulfanylpropanoate
英文别名
prop-2-ynyl 3-[3-[2,2-bis[3-(3-oxo-3-prop-2-ynoxypropyl)sulfanylpropanoyloxymethyl]butoxy]-3-oxopropyl]sulfanylpropanoate
Prop-2-ynyl 3-[3-[2,2-bis[3-(3-oxo-3-prop-2-ynoxypropyl)sulfanylpropanoyloxymethyl]butoxy]-3-oxopropyl]sulfanylpropanoate化学式
CAS
1224867-84-8
化学式
C33H44O12S3
mdl
——
分子量
728.903
InChiKey
XWJCKGVQPCRLIM-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):
    2.5
  • 重原子数:
    48
  • 可旋转键数:
    34
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.64
  • 拓扑面积:
    234
  • 氢给体数:
    0
  • 氢受体数:
    15

反应信息

  • 作为产物:
    参考文献:
    名称:
    Synthesis, Thiol−Yne “Click” Photopolymerization, and Physical Properties of Networks Derived from Novel Multifunctional Alkynes
    摘要:
    Multifunctional alkynes (2, 3, or 4 ynes per monomer) were prepared utilizing the nucleophile-catalyzed thio Michael addition reaction from commercially available multifunctional thiols (2, 3, or 4 thiols) and propargyl acrylate. Real-time FTIR (RTIR) and NMR spectroscopies indicate that the conjugate addition under these conditions proceeds to high conversions within seconds using the nucleophilic catalyst dimethylphenylphosphine, in the absence of solvent. at ambient temperature, and with no side products. A family of polymer networks was prepared by the photoinitiated thiol-yne reaction employing a 2:1 ratio of thiol to alkyne, which resulted in uniformly cross-linked materials of systematically increasing cross-link density. Photopolymerization kinetic profiles indicate that the thiol-yne reaction proceeded rapidly to high conversion with conversions decreasing with increasing functionality of the thiol and/or alkyne groups. Differential scanning calorimetry (DSC) and dynamic mechanical thermal analysis (DMTA) results clearly indicate that the glass transition temperature increases as the overall cross-link density increases (from -10 to 42 degrees C by DMTA). An increase in the rubbery modulus (from 6 to 23 MPa at 70 degrees C) results as the functionality increases, with a concomitant decrease in the molecular weight between cross-links.
    DOI:
    10.1021/ma1004452
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文献信息

  • UV curable inkjet inks
    申请人:AGFA NV
    公开号:US10513620B2
    公开(公告)日:2019-12-24
    An aqueous UV free radical curable inkjet ink contains a liquid phase A dispersed in a continuous liquid phase B by a polymeric dispersant; wherein the liquid phase A contains at least a photoinitiator, a colour pigment, and one or more polymerizable compounds, and the continuous liquid phase B contains water and optionally one or more organic solvents.
    一种性紫外线自由基固化喷墨墨含有通过聚合物分散剂分散在连续液相 B 中的液相 A;其中液相 A 至少含有光引发剂、彩色颜料和一种或多种可聚合化合物,连续液相 B 含有和可选的一种或多种有机溶剂。
  • UV CURABLE INKJET INKS
    申请人:AGFA NV
    公开号:EP3156461B1
    公开(公告)日:2020-04-01
  • [EN] UV CURABLE INKJET INKS<br/>[FR] ENCRES POUR JET D'ENCRE DURCISSABLES PAR UV
    申请人:AGFA GRAPHICS NV
    公开号:WO2017063968A1
    公开(公告)日:2017-04-20
    An aqueous UV curable inkjet ink containing: a) an aqueous medium; b) a photoinitiator (3); c) a thiol compound (4,6) including at least two thiol groups; d) polymeric particles (1) containing a polymer, an oligomer or a monomer having ethylenically unsaturated polymerizable groups; and e) optionally a colorant (2).
  • [EN] UV CURABLE INKJET INKS<br/>[FR] ENCRES À JET D'ENCRE DURCISSABLES PAR UV
    申请人:AGFA GRAPHICS NV
    公开号:WO2017063983A1
    公开(公告)日:2017-04-20
    An aqueous UV curable inkjet ink (1) including a) an aqueous medium (2); and b) capsules (3) composed of a polymeric shell (4) surrounding a core (5) containing one or more polymerizable compounds having an alkyne group or an ethylenically unsaturated group; wherein the aqueous UV curable inkjet ink contains one or more photoinitiators and one or more thiol compounds having at least two thiol groups.
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