6-chloro-3-methyl-2-methylsulfanyl-benzothiazolium; iodide | 20065-00-3

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并噻唑类
• 英文名称: 6-chloro-3-methyl-2-methylsulfanyl-benzothiazolium; iodide
• 英文别名: 6-Chloro-3-methyl-2-methylsulfanyl-1,3-benzothiazol-3-ium;iodide
• CAS: 20065-00-3
• 化学式: C₉H₉ClNS₂*I
• 分子量: 357.667
• InChiKey: UCSPXLSSERMDCK-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  0.11
• 重原子数：
  14
• 可旋转键数：
  1
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.22
• 拓扑面积：
  57.4
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  6-chloro-3-methyl-2-methylsulfanyl-benzothiazolium; iodide 在 一水合肼 作用下， 以 水 为溶剂， 反应 4.0h， 生成 6-chloro-2-(8-hydroxy-quinolin-5-ylazo)-3-methyl-benzothiazolium; iodide
  参考文献：
  名称：

  Mohanty,S. et al., Indian Journal of Chemistry, 1968, vol. 6, p. 136 - 139

  摘要：

  DOI：

文献信息

• Class of cyano-substituted asymmetric cyanine dyes, synthesizing method and application thereof
  申请人：DALIAN UNIVERSITY OF TECHNOLOGY

  公开号：US10029996B2

  公开（公告）日：2018-07-24

  The present invention provides a category of cyano-substituted asymmetric cyanine dyes having the following general structural Formula I and its synthesizing method. The cyano-substituted asymmetric cyanine dyes in present invention are easily synthesized and have long emission wavelength, high molar extinction coefficient, high sensitivity, good light stability, high fluorescence quantum yield after binding with nucleic acid, and low cell toxicity, which is beneficial for application as fluorescent dyes and could also be used in the field of identifying nucleic acid molecules, clinical diagnostics, and immunoassay testing etc.

  本发明提供了一类具有以下一般结构式I和其合成方法的氰基取代不对称青光菁染料。本发明中的氰基取代不对称青光菁染料易于合成，具有长的发射波长、高的摩尔消光系数、高的灵敏度、良好的光稳定性、与核酸结合后高的荧光量子产率和低的细胞毒性，有利于作为荧光染料应用，并可用于鉴定核酸分子、临床诊断和免疫测定等领域。
• [EN] PESTICIDAL CYANINE DYE DERIVATIVES<br/>[FR] DERIVES PESTICIDES DE COLORANTS CYANINE
  申请人：FMC CORP

  公开号：WO2004010761A2

  公开（公告）日：2004-02-05

  Cyanine dye derivatives provide unexpected pesticidal activity. These compounds are represented by formula (I): where Ar, Ar1, p, q, r, and R through R4, inclusively, are described. Preferred compounds of formula I include those where Ar is (II); and AR1 is (III); (IV); or (V); where X, Y, Z X2, Y2, Z2, R5, R17 through R27, inclusively, are described. Compositions comprising a pesticidally effective amount of at least one compound of formula I, and optionally, an effective amount of at least one of a second pesticidally active compound, with at least one pesticidally compatible carrier are also disclosed; along with methods of controlling pests comprising applying said compositions to a locus where pests are present or are expected to be present. The compositions of the present invention are of particular interest for their insecticidal and acaricidal activity.
• Mohanty,S. et al., Indian Journal of Chemistry, 1968, vol. 6, p. 136 - 139
  作者：Mohanty,S. et al.

  DOI：——

  日期：——