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2,4,6-三(2-丙炔-1-氧基)-1,3,5-三嗪 | 15911-93-0

中文名称
2,4,6-三(2-丙炔-1-氧基)-1,3,5-三嗪
中文别名
——
英文名称
2,4,6-tris(prop-2-ynyloxy)-1,3,5-triazine
英文别名
2,4,6-tris-prop-2-ynyloxy-[1,3,5]triazine;2,4,6-tris(2-propynyloxy)-1,3,5-triazine;2,4,6-tris(propargyloxy)-1,3,5-triazine;2,4,6-tris(prop-2-ynyl)-1,3,5-triazine;2,4,6-tripropargyloxy-1,3,5-triazine;2,4,6-Tris-(2-propinyloxy)-s-triazin;2,4,6-Tris(prop-2-yn-1-yloxy)-1,3,5-triazine;2,4,6-tris(prop-2-ynoxy)-1,3,5-triazine
2,4,6-三(2-丙炔-1-氧基)-1,3,5-三嗪化学式
CAS
15911-93-0
化学式
C12H9N3O3
mdl
MFCD00441828
分子量
243.222
InChiKey
DRFJNVUYUQQIDX-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:
    79.5-80.5 °C
  • 沸点:
    378.8±52.0 °C(Predicted)
  • 密度:
    1.270±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    18
  • 可旋转键数:
    6
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.25
  • 拓扑面积:
    66.4
  • 氢给体数:
    0
  • 氢受体数:
    6

安全信息

  • 海关编码:
    2933699090

SDS

SDS:2f02829cb781c26c1ff60662cbff767e
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上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    参考文献:
    名称:
    Cyanuric and thiocyanuric esters as carriers of boron-containing fragments and their fragmentation in mass spectrometry
    摘要:
    Tripropargylic esters 2 and 10 of cyanuric and thiocyanuric acids were synthesized. Interaction of these compounds with disubstituted amines gives monoaminoderivatives of dipropargyloxy-s-triazine 4 and 11. Diamino substituted propargyloxy-s-triazine 6 was prepared from the corresponding diaminochloroderivative 5. First examples of boron-containing s-triazines 7, 8, 12, 13 were prepared by reaction of propargyl esters 4, 6, 10, 11 with decaborane. New rearrangements of the molecular ions of the 2-aminoderivatives of 4,6-dipropargyloxy-1,3,5-triazine in mass spectrometry were found. (C) 2003 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2003.09.153
  • 作为产物:
    描述:
    三聚氯氰2-丙炔-1-醇potassium carbonate 作用下, 以 四氢呋喃 为溶剂, 以90%的产率得到2,4,6-三(2-丙炔-1-氧基)-1,3,5-三嗪
    参考文献:
    名称:
    通过无铜热惠斯根反应稳定电光聚合物中发色团取向的更简单,更有效的策略
    摘要:
    提出了一种新策略,该策略使用无铜热惠斯根1,3-偶极子交联反应稳定二阶材料的电光(EO)活性。其在于在极化过程之后通过基于叠氮化物和炔烃之间的1,3-偶极环加成的交联反应来冻结发色团的取向。为了达到这个目标,进行了带有分散红1发色团衍生物的新型甲基丙烯酸酯型聚合物的合成。聚合物结构在其主链上具有可交联的功能,而互补的反应性功能则由称为“掺杂剂”(DA)的小分子带来),含有几个互补的交联基团,均匀分布在聚合物薄膜中。已经制备了材料,并且在1064 nm的基本波长下具有高达60 pm / V的大二阶非线性光学系数(d 33)。而且,在与这些材料交联时,生色团的取向的热稳定性可以达到150℃,这高于基于该反应的先前描述的可交联的EO聚合物。此外,这种新策略拓宽了无铜热惠斯根1,3-偶极环加成作为EO聚合物的交联反应的可能性。
    DOI:
    10.1016/j.polymer.2011.02.042
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文献信息

  • Synthesis of Podands with Cyanurate or Isocyanurate Cores and Terminal Triple Bonds
    作者:Crina Cismaş、Ion Grosu、Flavia Piron、Cornelia Oprea、Anamaria Terec、Jean Roncali
    DOI:10.1055/s-0029-1218724
    日期:2010.5
    The synthesis of podands with cyanuric or isocyanuric acid cores and oligoethyleneoxy pendant arms exhibiting terminal triple bonds or brominated triple bonds is reported. The starting material for cyanuric acid derived podands is commercially available cyanuric acid, while the isocyanuric derivatives are obtained by thermal isomerization of the corresponding cyanurates.
    报告了以氰尿酸或异氰尿酸核为核心、带有末端三键或溴化三键的聚氧乙烯侧臂的穴状配体合成。氰尿酸衍生穴状配体的起始原料为市售氰尿酸,而异氰尿酸衍生物则通过相应氰尿酸盐的热异构化获得。
  • Design of novel photosensitizers and controlled singlet oxygen generation for photodynamic therapy
    作者:Esra Tanrıverdi Eçik、Onur Bulut、Hasan Huseyin Kazan、Elif Şenkuytu、Bünyemin Çoşut
    DOI:10.1039/d1nj02656a
    日期:——
    times higher than that of compound 6. The photosensitizer (5), bearing iodinated BODIPY units, exhibited almost a non-fluorescent profile with a fluorescence lifetime of 0.12 ns, whereas the other photosensitizer (6) exhibited a more moderate fluorescence character with a fluorescence lifetime of 1.22 ns. The singlet oxygen quantum yields of the photosensitizers were determined to be 0.88 and 0.76, respectively
    光动力疗法 (PDT) 是一种有前景的癌症治疗策略,其副作用相对较低。毫无疑问,PDT的关键成分是具有高单线态氧产生能力的光敏剂。在这项工作中,碘化或溴化硼二吡咯亚甲基三聚体(5和6)被制备为光敏剂,并通过质谱和核磁共振(1 H 和13 C)光谱表征了它们的分子结构。还详细评估了它们的光物理和光化学能力。摩尔吸光系数(ε化合物的)5被发现是比化合物的高2.5倍6。光敏剂(带有碘化 BODIPY 单元的图5 ) 表现出几乎无荧光的特征,荧光寿命为 0.12 ns,而其他光敏剂 ( 6 ) 表现出更温和的荧光特征,荧光寿命为 1.22 ns。通过化学捕获法测定光敏剂的单线态氧量子产率分别为 0.88 和 0.76。此外,新化合物的生物学评估表明,这些 PSs 被内化到细胞中并以依赖光源的方式引发细胞死亡,这是化合物在体外PDT中取得成功的基础。
  • PHOTOCURING METHOD, COMPOUND AND COMPOSITION USED THEREIN
    申请人:FUJIFILM Wako Pure Chemical Corporation
    公开号:US20190055210A1
    公开(公告)日:2019-02-21
    An object of the present invention is to provide a photocuring method, which makes it possible to rapidly and efficiently obtain a crosslinked product (resin), a compound used in the photocuring method, and a photocuring resin composition containing the compound. The present invention relates to a photocuring method, which comprises a step 1 and a step 2 performed after the step 1, a compound used in the photocuring method, and a photocuring resin composition containing the compound. Step 1: this is a step in which in the presence of (A) compound having a carbonyl group generating a radical by photoirradiation and a carboxyl group decarboxylated by photoirradiation, (B) silane coupling agent having a mercapto group or a (meth)acryl group is reacted with (C) water under acidic conditions to obtain (D) silane compound having a mercapto group or a (meth)acryl group and at least one silanol group. Step 2: this is a step in which in the presence of the compound (A) and (E) compound having a carbonyl group generating a radical by photoirradiation and a group generating a base by being decarboxylated by photoirradiation, the compound (A) and the compound (E) are irradiated with light to create alkaline conditions in a reaction system by decarboxylating the carboxyl group of the compound (A) and generating a base from the compound (E), and radicals are generated from the compound (A) and the compound (E) to generate a crosslinked product containing a constitutional unit derived from the silane compound (D) from the silane compound (D) and, if necessary, from (F) compound having two or more polymerizable unsaturated groups.
    本发明的一个目标是提供一种光固化方法,该方法使得能够快速高效地获得交联产物(树脂),以及用于光固化方法的化合物和含有该化合物的光固化树脂组合物。本发明涉及一种光固化方法,该方法包括在步骤1和步骤2之后执行的步骤1和步骤2,以及用于光固化方法的化合物和含有该化合物的光固化树脂组合物。步骤1:这是一个步骤,在该步骤中,在(A)具有通过光照生成自由基的羰基和通过光照脱羧生成羧基的化合物的存在下,(B)具有巯基或(甲基)丙烯基的硅烷偶联剂在酸性条件下与(C)水反应,以获得具有巯基或(甲基)丙烯基和至少一个硅醇基团的(D)硅烷化合物。步骤2:这是一个步骤,在该步骤中,在化合物(A)和(E)具有通过光照生成自由基的羰基和通过光照脱羧生成碱基的化合物的存在下,通过照射光线使化合物(A)和化合物(E)在反应系统中产生碱性条件,通过脱羧化合物(A)的羧基并从化合物(E)中生成碱基,并从化合物(A)和化合物(E)中生成自由基,从而生成包含从硅烷化合物(D)派生的构造单元的交联产物,如果需要,还可以从具有两个或更多可聚合不饱和基团的化合物(F)中派生。
  • [EN] ANIONIC CONJUGATES OF GLYCOSYLATED BACTERIAL METABOLITE<br/>[FR] CONJUGUÉS ANIONIQUES D'UN MÉTABOLITE BACTÉRIEN GLYCOSYLÉ
    申请人:GLYCAN BIOSCIENCES PTY LTD
    公开号:WO2010037179A1
    公开(公告)日:2010-04-08
    The invention relates to anionic conjugates of glycosylated bacterial metabolites that may be used to mimic the structure and/or activity of the anionic bioactive molecules known as glycosaminoglycans (GAGs). The invention also relates to processes for the preparation of the conjugates. Such conjugates are useful in the prophylaxis and/or treatment of disease conditions and in particular chronic disease conditions such as inflammatory (including allergic) diseases, metastatic cancers and infection by pathogenic agents including bacteria, viruses or parasites.
    该发明涉及与糖基化细菌代谢产物的阴离子结合物,可用于模拟被称为糖胺聚糖(GAGs)的阴离子生物活性分子的结构和/或活性。该发明还涉及制备这些结合物的过程。这些结合物在预防和/或治疗疾病条件方面具有用处,特别是慢性疾病条件,如炎症(包括过敏)疾病、转移性癌症和感染病原体(包括细菌、病毒或寄生虫)的情况。
  • Synthesis of Fan-Shaped <i>C</i> <sub>3</sub> Molecule with Three Glycyrrhetinic Acid Units and Self-Assembly Properties
    作者:Jun Hu、Libing Yu、Meng Zhang、Yong Ju
    DOI:10.1002/cjoc.201190213
    日期:2011.6
    A novel fan‐shaped C3 molecule with three glycyrrhetinic acid units was synthesized via "click chemistry" in high yield and the self‐assembly characteristics were studied in different mixed solvents.
    通过“点击化学”以高收率合成了具有三个甘草次酸单元的新型扇形C 3分子,并研究了其在不同混合溶剂中的自组装特性。
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