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4-[(Z)-2-[(3E)-2-chloro-3-[(2E)-2-(2-phenylthiochromen-4-ylidene)ethylidene]cyclohexen-1-yl]ethenyl]-2-phenylthiochromenylium;perchlorate | 76871-75-5

中文名称
——
中文别名
——
英文名称
4-[(Z)-2-[(3E)-2-chloro-3-[(2E)-2-(2-phenylthiochromen-4-ylidene)ethylidene]cyclohexen-1-yl]ethenyl]-2-phenylthiochromenylium;perchlorate
英文别名
——
4-[(Z)-2-[(3E)-2-chloro-3-[(2E)-2-(2-phenylthiochromen-4-ylidene)ethylidene]cyclohexen-1-yl]ethenyl]-2-phenylthiochromenylium;perchlorate化学式
CAS
76871-75-5
化学式
C40H30Cl2O4S2
mdl
——
分子量
709.7
InChiKey
UQPOJGGXKFKEGG-UHFFFAOYSA-M
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

  • 密度:
    1.3253 (estimate)
  • 稳定性/保质期:

    遵照规定使用和储存,则不会分解。

计算性质

  • 辛醇/水分配系数(LogP):
    7.94
  • 重原子数:
    48
  • 可旋转键数:
    5
  • 环数:
    7.0
  • sp3杂化的碳原子比例:
    0.07
  • 拓扑面积:
    128
  • 氢给体数:
    0
  • 氢受体数:
    5

安全信息

  • 危险等级:
    5.1
  • 危险品标志:
    F
  • 安全说明:
    S16
  • 危险类别码:
    R11
  • 包装等级:
    III
  • 危险类别:
    5.1

文献信息

  • High resolution imaging using near-infrared-II fluorescence
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US10264974B2
    公开(公告)日:2019-04-23
    Disclosed are methods for imaging lumen-forming structures such as blood vessels using near-infrared fluorescence in the NIR-II region of 1000-1700 nm. The fluorescence is created by excitation of solubilized nano-structures that are delivered to the structures, such as carbon nanotubes, quantum dots or organic molecular fluorophores attached to hydrophilic polymers. These nanostructures fluoresce in the NIR-II region when illuminated through the skin and tissues. Fine anatomical vessel resolution down to −30 μm and high temporal resolution up to 5-10 frames per second is obtained for small-vessel imaging with up to 1 cm penetration depth in mouse hind limb, which compares favorably to tomographic imaging modalities such as CT and MRI with much higher spatial and temporal resolution, and compares favorably to scanning microscopic imaging techniques with much deeper penetration.
    所公开的是利用 1000-1700 纳米 NIR-II 区域的近红外荧光对血管等管腔形成结构进行成像的方法。荧光是通过激发溶解的纳米结构产生的,这些纳米结构被输送到结构中,如碳纳米管、量子点或附着在亲水性聚合物上的有机分子荧光团。通过皮肤和组织照射时,这些纳米结构会在近红外-II 区发出荧光。在小鼠后肢穿透深度达 1 厘米的小血管成像中,可获得低至 -30 μm 的精细解剖血管分辨率和高达每秒 5-10 帧的高时间分辨率,与空间和时间分辨率更高的 CT 和 MRI 等断层成像模式相比毫不逊色,与穿透深度更深的扫描显微成像技术相比也毫不逊色。
  • COMPOSITIONS AND METHODS FOR CREATING ELECTRONIC CIRCUITRY
    申请人:LEE YUEH-LING
    公开号:US20100009173A1
    公开(公告)日:2010-01-14
    The present invention is directed to non-lithographic patterning by laser (or similar-type energy beam) ablation, where the ablation system ultimately results in circuitry features that are relative free from debris induced over-plating defects (debris relating to the ablation process) and fully additive plating induced over-plating defects. Compositions of the invention include a circuit board precursor having an insulating substrate and a cover layer. The insulating substrate is made from a dielectric material and also a metal oxide activatable filler. The cover layer can be sacrificial or non-sacrificial and is used to remediate unwanted debris arising from the ablation process.
  • HIGH RESOLUTION IMAGING USING NEAR-INFRARED-II FLUORESCENCE
    申请人:The Board of Trustees of the Leland Stanford Junior University
    公开号:US20150297086A1
    公开(公告)日:2015-10-22
    Disclosed are methods for imaging lumen-forming structures such as blood vessels using near-infrared fluorescence in the NIR-II region of 1000-1700 nm. The fluorescence is created by excitation of solubilized nano-structures that are delivered to the structures, such as carbon nanotubes, quantum dots or organic molecular fluorophores attached to hydrophilic polymers. These nanostructures fluoresce in the NIR-II region when illuminated through the skin and tissues. Fine anatomical vessel resolution down to −30 μm and high temporal resolution up to 5-10 frames per second is obtained for small-vessel imaging with up to 1 cm penetration depth in mouse hind limb, which compares favorably to tomographic imaging modalities such as CT and MRI with much higher spatial and temporal resolution, and compares favorably to scanning microscopic imaging techniques with much deeper penetration.
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