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1-氯-2-(2-碘-乙氧基)乙烷 | 42070-18-8

中文名称
1-氯-2-(2-碘-乙氧基)乙烷
中文别名
——
英文名称
1-Chlor-5-iod-3-oxapentan
英文别名
1-(2-chloro-ethoxy)-2-iodo-ethane;2-chloro-ethyl 2-iodo-ethyl ether;1-Chloro-2-(2-iodoethoxy)ethane
1-氯-2-(2-碘-乙氧基)乙烷化学式
CAS
42070-18-8
化学式
C4H8ClIO
mdl
——
分子量
234.464
InChiKey
XXUFCDWWUANVRH-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):
    1.8
  • 重原子数:
    7
  • 可旋转键数:
    4
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    1.0
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 包装等级:
    III
  • 危险类别:
    6.1
  • 危险性防范说明:
    P201,P202,P261,P264,P270,P271,P280,P302+P352,P304+P340,P308+P313,P310,P330,P361,P403+P233,P405,P501
  • 危险品运输编号:
    2810
  • 危险性描述:
    H301,H311,H331,H341

反应信息

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文献信息

  • Syntheses, optical properties, and bioapplications of the aggregation-induced emission of 2,3,4,5-tetraphenylcyclopenta-2,4-dienyl benzene derivatives
    作者:Franklin Anariba、Leng Leng Chng、Nur Sharalyn Abdullah、Francis E. H. Tay
    DOI:10.1039/c2jm32755d
    日期:——
    Syntheses of 2,3,4,5-tetraphenylcyclopenta-2,4-dienyl benzene derivatives tailored with seven substituents of various lengths and molecular composition were accomplished and their UV-Vis and fluorescence properties investigated. All of the novel fluorescent dyes displayed varying degrees of aggregation-induced emission (AIE) in the blue region of ∼460 nm in various organic and aqueous solvents. Interestingly, the studies revealed the novel ability of this family of molecules to show strong luminescence in both organic solvents (e.g., %Φf = 69.0% in toluene) and aqueous solutions (e.g., %Φf = 14.0% in H2O) without the need to mix organic and aqueous solvents. Furthermore, fluorescence properties as a function of temperature indicated that both aggregation-induced behavior and the initial degree of solubility played an important role in the overall observed properties of the fluorescent dyes. The importance of this family of molecules for nucleic acid detection and bioimaging applications was demonstrated via the “turn off” detection of cDNA and ss-DNA and by successful tagging and imaging of lens epithelial cells. Taken together, these findings are of great importance for they provide a platform for further rational design and synthesis of luminescent (due to aggregation-induced) and biocompatible (non-toxic) nanoparticles for a wide range of imaging and sensory applications.
    我们合成了由七个不同长度和分子组成的取代基定制的 2,3,4,5- 四苯基环戊-2,4-二烯苯衍生物,并研究了它们的紫外可见光和荧光特性。在各种有机溶剂和溶剂中,所有新型荧光染料在 ∼460 纳米的蓝色区域都显示出不同程度的聚集诱导发射(AIE)。有趣的是,研究揭示了这一分子家族的新能力,即在有机溶剂中(如在甲苯中,%Φf = 69.0%)和溶液中(如在 H2O 中,%Φf = 14.0%)都能显示出强烈的发光,而无需混合有机溶剂和溶液。此外,荧光特性与温度的函数关系表明,聚合引起的行为和初始溶解度对荧光染料的整体观察特性起着重要作用。通过对 cDNA 和 ss-DNA 的 "关闭 "检测,以及对晶状体上皮细胞的成功标记和成像,证明了这一系列分子在核酸检测和生物成像应用方面的重要性。总之,这些发现非常重要,因为它们为进一步合理设计和合成发光(由于聚集诱导)和生物相容性(无毒)纳米粒子提供了一个平台,可用于广泛的成像和感官应用。
  • Alkyloxy Substituted Thiazoloquinolines and Thiazolonaphthyridines
    申请人:Prince Ryan B.
    公开号:US20080318998A1
    公开(公告)日:2008-12-25
    Thiazoloquinolines and thiazolonaphthyridines with an alkoxy substituent at the 6, 7, 8, or 9-position, pharmaceutical compositions containing the compounds, intermediates, methods of making and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.
    本发明公开了在6、7、8或9位具有烷氧基取代基的噻唑喹啉噻唑啶,包含这些化合物的制药组合物、中间体、制备方法以及这些化合物作为免疫调节剂的使用方法,用于诱导动物细胞因子生物合成和治疗包括病毒和肿瘤疾病的疾病。
  • ALKYLOXY SUBSTITUTED THIAZOLOQUINOLINES AND THIAZOLONAPHTHYRIDINES
    申请人:3M INNOVATIVE PROPERTIES COMPANY
    公开号:US20150266901A1
    公开(公告)日:2015-09-24
    Thiazoloquinolines and thiazolonaphthyridines with an alkoxy substituent at the 6, 7, 8, or 9-position, pharmaceutical compositions containing the compounds, intermediates, methods of making and methods of use of these compounds as immunomodulators, for inducing cytokine biosynthesis in animals and in the treatment of diseases including viral and neoplastic diseases are disclosed.
    本文披露了在6、7、8或9位具有烷氧基取代基的噻唑喹啉噻唑啶类化合物、含有这些化合物的制药组合物、中间体、制备方法以及这些化合物作为免疫调节剂的用途、用于诱导动物细胞因子生物合成和用于治疗包括病毒和肿瘤疾病在内的疾病的方法。
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