5-vinyl-1,3-dihydro-benzo[c]thiophene-2,2-dioxide | 881880-92-8

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 英文名称: 5-vinyl-1,3-dihydro-benzo[c]thiophene-2,2-dioxide
• 英文别名: 5-Ethenyl-1,3-dihydro-2H-2-benzothiophene-2,2-dione；5-ethenyl-1,3-dihydro-2-benzothiophene 2,2-dioxide
• CAS: 881880-92-8
• 化学式: C₁₀H₁₀O₂S
• 分子量: 194.254
• InChiKey: KHWQITFBSAZENY-UHFFFAOYSA-N

物化性质

• 沸点：
  425.2±45.0 °C(Predicted)
• 密度：
  1.286±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  13
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  42.5
• 氢给体数：
  0
• 氢受体数：
  2

反应信息

• 作为产物：
  描述：

  5-trimethylsilylvinyl-1,3-dihydro-benzo[c]thiophene-2,2-dioxide 在 三氟乙酸 作用下， 以 二氯甲烷 为溶剂， 反应 14.0h， 以93.2%的产率得到5-vinyl-1,3-dihydro-benzo[c]thiophene-2,2-dioxide
  参考文献：
  名称：

  WO2008/24435

  摘要：

  公开号：

文献信息

• DENDRITIC MOLECULAR INTRACELLULAR TRANSPORTERS AND METHODS OF MAKING AND USING SAME
  申请人：Harth Eva M.

  公开号：US20080221043A1

  公开（公告）日：2008-09-11

  In accordance with the purpose(s) of the invention, as embodied and broadly described herein, the invention, in one aspect, relates to compounds comprising the structure: and at least one guanidinium residue, wherein m is zero or a positive integer. Also disclosed are methods of preparing the disclosed compounds. Also disclosed are methods of intracellular delivery comprising administering the disclosed compounds and compositions to a subject. Also disclosed are pharmaceutical compositions comprising a therapeutically effective amount of one or more compounds or compositions of the invention and a pharmaceutically acceptable carrier. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  根据本发明的目的，本发明在一个方面涉及包含以下结构的化合物，以及至少一个鸟氨酸残基，其中m为零或正整数。还公开了制备所述化合物的方法。还公开了包括将所述化合物和组合物给予受试者的细胞内递送方法。还公开了包括本发明的一个或多个化合物或组合物的治疗有效量和药学可接受载体的制药组合物。本摘要旨在作为搜索特定领域的扫描工具，不限制本发明。
• MULTIFUNCTIONAL DEGRADABLE NANOPARTICLES WITH CONTROL OVER SIZE AND FUNCTIONALITIES
  申请人：Harth Eva M.

  公开号：US20090306335A1

  公开（公告）日：2009-12-10

  In one aspect, the invention relates to polymers, crosslinked polymers, functionalized polymers, nanoparticles, and functionalized nanoparticles and methods of making and using same. In one aspect, the invention relates to degradable polymer and degradable nanoparticles. In one aspect, the invention relates to methods of preparing degradable nanoparticles and, more specifically, methods of controlling particle size during the preparation of degradable nanoparticles. In one aspect, the degradable nanoparticles are useful for complexing, delivering, and releasing payloads, including pharmaceutically active payloads. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  本发明涉及聚合物、交联聚合物、功能化聚合物、纳米颗粒和功能化纳米颗粒以及其制备和使用方法。其中，本发明涉及可降解聚合物和可降解纳米颗粒。本发明还涉及制备可降解纳米颗粒的方法，更具体地说，涉及在制备可降解纳米颗粒过程中控制颗粒大小的方法。在一方面，这些可降解纳米颗粒可用于复合、传递和释放药物活性载荷等方面。本摘要旨在作为搜索特定技术领域的扫描工具，不限制本发明。
• Multifunctional degradable nanoparticles with control over size and functionalities
  申请人：Vanderbilt University

  公开号：US07935782B2

  公开（公告）日：2011-05-03

  In one aspect, the invention relates to polymers, crosslinked polymers, functionalized polymers, nanoparticles, and functionalized nanoparticles and methods of making and using same. In one aspect, the invention relates to degradable polymer and degradable nanoparticles. In one aspect, the invention relates to methods of preparing degradable nanoparticles and, more specifically, methods of controlling particle size during the preparation of degradable nanoparticles. In one aspect, the degradable nanoparticles are useful for complexing, delivering, and releasing payloads, including pharmaceutically active payloads. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  在一个方面，本发明涉及聚合物、交联聚合物、功能化聚合物、纳米颗粒和功能化纳米颗粒的制备和使用方法。在一个方面，本发明涉及可降解聚合物和可降解纳米颗粒。在一个方面，本发明涉及制备可降解纳米颗粒的方法，更具体地说，是在制备可降解纳米颗粒的过程中控制颗粒大小的方法。在一个方面，可降解纳米颗粒可用于复合、传递和释放药物活性载荷等用途。本摘要旨在作为搜索特定技术领域的扫描工具，不限制本发明。
• Multifunctional Degradable Nanoparticles with Control over Size and Functionalities
  申请人：Harth Eva M.

  公开号：US20110257343A1

  公开（公告）日：2011-10-20

  In one aspect, the invention relates to polymers, crosslinked polymers, functionalized polymers, nanoparticles, and functionalized nanoparticles and methods of making and using same. In one aspect, the invention relates to degradable polymer and degradable nanoparticles. In one aspect, the invention relates to methods of preparing degradable nanoparticles and, more specifically, methods of controlling particle size during the preparation of degradable nanoparticles. In one aspect, the degradable nanoparticles are useful for complexing, delivering, and releasing payloads, including pharmaceutically active payloads. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  一方面，本发明涉及聚合物、交联聚合物、功能化聚合物、纳米颗粒和功能化纳米颗粒的制备和使用方法。另一方面，本发明涉及可降解聚合物和可降解纳米颗粒。另一方面，本发明涉及制备可降解纳米颗粒的方法，更具体地说，涉及在制备可降解纳米颗粒过程中控制颗粒大小的方法。另一方面，可降解纳米颗粒可用于复合、传递和释放药物活性载荷等用途。本摘要旨在作为搜索特定领域的扫描工具，不限制本发明。
• Dendritic molecular intracellular transporters and methods of making and using same
  申请人：Harth Eva M.

  公开号：US08969622B2

  公开（公告）日：2015-03-03

  In accordance with the purpose(s) of the invention, as embodied and broadly described herein, the invention, in one aspect, relates to compounds comprising the structure: and at least one guanidinium residue, wherein m is zero or a positive integer. Also disclosed are methods of preparing the disclosed compounds. Also disclosed are methods of intracellular delivery comprising administering the disclosed compounds and compositions to a subject. Also disclosed are pharmaceutical compositions comprising a therapeutically effective amount of one or more compounds or compositions of the invention and a pharmaceutically acceptable carrier. This abstract is intended as a scanning tool for purposes of searching in the particular art and is not intended to be limiting of the present invention.

  根据本发明的目的，如本文所体现和广泛描述的，本发明在一个方面涉及包含以下结构和至少一个鸟氨酸残基的化合物，其中m为零或正整数。还披露了制备所述化合物的方法。还披露了将所述化合物和组合物给予受试者进行细胞内递送的方法。还披露了包含本发明中一种或多种化合物或组合物的治疗有效量和药学可接受载体的制药组合物。此摘要旨在作为特定领域搜索的扫描工具，不旨在限制本发明。