2-methyl-5-(2,4,6-trinitro-styryl)-thiophene

• 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: 2-methyl-5-(2,4,6-trinitro-styryl)-thiophene
• 英文别名: 2-Methyl-5-(2,4,6-trinitro-styryl)-thiophen；2,4,6-trinitrostyryl-5-methylthiophene；2-methyl-5-[(E)-2-(2,4,6-trinitrophenyl)ethenyl]thiophene
• 化学式: C₁₃H₉N₃O₆S
• 分子量: 335.297
• InChiKey: OPHHNTQSRSCJGU-SNAWJCMRSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  3.8
• 重原子数：
  23
• 可旋转键数：
  2
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.08
• 拓扑面积：
  166
• 氢给体数：
  0
• 氢受体数：
  7

反应信息

• 作为产物：
  描述：

  2-甲基噻吩 在 哌啶 、 三氯氧磷 、 苯 作用下， 生成 2-methyl-5-(2,4,6-trinitro-styryl)-thiophene
  参考文献：
  名称：

  Buu-Hoi et al., Journal of the Chemical Society, 1950, p. 2130,2134

  摘要：

  DOI：

文献信息

• Analyte detection and apparatus therefor
  申请人：——

  公开号：US20040234958A1

  公开（公告）日：2004-11-25

  The present invention relates to sensitive SE(R)RS based methods for detecting analytes such as explosives and drugs, which may be present in a sample at extremely low levels. The methods may be generally carried out in situ employing novel chemistry which is compatible with flow-cell technology and with time-scales and concentrations required for rapid and informative screening of large numbers of samples. The present invention also relates to novel compounds e.g. synthons and apparatus for use with the methods disclosed.

  本发明涉及基于敏感SE（R）RS的方法，用于检测可能以极低水平存在于样本中的爆炸物和药物等分析物。这些方法通常可以在原位进行，采用与流动池技术兼容的新型化学物质，以及快速和信息性筛选大量样本所需的时间尺度和浓度。本发明还涉及用于所披露方法的新型化合物，例如合成物和装置。
• ANALYTE DETECTION
  申请人：University of Strathclyde

  公开号：EP1272827B1

  公开（公告）日：2008-09-17
• ANALYTE DETECTION & APPARATUS THEREFOR
  申请人：UNIVERSITY OF STRATHCLYDE

  公开号：EP1272827A1

  公开（公告）日：2003-01-08
• US7741102B2
  申请人：——

  公开号：US7741102B2

  公开（公告）日：2010-06-22
• [EN] ANALYTE DETECTION & APPARATUS THEREFOR<br/>[FR] DETECTION D'ANALYTE ET APPAREIL ASSOCIE
  申请人：UNIV STRATHCLYDE

  公开号：WO2001077650A1

  公开（公告）日：2001-10-18

  The present invention relates to sensitive SE(R)RS based methods for detecting analytes such as explosives and drugs, which may be present in a sample at extremely low levels. The methods may be generally carried out in situ employing novel chemistry which is compatible with flow-cell technology and with time-scales and concentrations required for rapid and informative screening of large numbers of samples. The present invention also relates to novel compounds e.g. synthons and apparatus for use with the methods disclosed.