Spiro[1,3,3a,6,7,7a-hexahydroindene-2,3'-oxolane]-1-ol

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 四氢呋喃
• 英文名称: Spiro[1,3,3a,6,7,7a-hexahydroindene-2,3'-oxolane]-1-ol
• 英文别名: spiro[1,3,3a,6,7,7a-hexahydroindene-2,3'-oxolane]-1-ol
• 化学式: C₁₂H₁₈O₂
• 分子量: 194.27
• InChiKey: YCQMUMQHXFDRKH-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.4
• 重原子数：
  14
• 可旋转键数：
  0
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.83
• 拓扑面积：
  29.5
• 氢给体数：
  1
• 氢受体数：
  2

文献信息

• [EN] SUBSTITUTED TOLYL FUNGICIDE MIXTURES<br/>[FR] MÉLANGES FONGICIDES DE DÉRIVÉS DE TOLYLE
  申请人：DU PONT

  公开号：WO2015157005A1

  公开（公告）日：2015-10-15

  Disclosed is a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1, N-oxides, and salts thereof, wherein A, Q, R1 and R2 are as defined in the disclosure; and (b) at least one additional fungicidal compound selected from those disclosed herein. Also disclosed is a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of the aforesaid composition.

  本发明公开了一种杀真菌组合物，包括（a）至少一种选择自化合物式1、N-氧化物和其盐的化合物，其中A、Q、R1和R2如本公开中所定义；以及（b）至少一种从本文所披露的其他杀真菌化合物中选择的额外杀真菌化合物。还公开了一种控制由真菌植物病原体引起的植物疾病的方法，包括向植物或其部分，或向植物种子施用上述组合物中的杀真菌有效量。
• [EN] FUNGICIDAL PYRAZOLE MIXTURES<br/>[FR] MÉLANGES DE PYRAZOLES FONGICIDES
  申请人：DU PONT

  公开号：WO2014130409A2

  公开（公告）日：2014-08-28

  Disclosed is a fungicidal composition comprising (a) at least one compound selected from the compounds of Formula 1, N-oxides, and salts thereof, (1) wherein R1 is H or halogen; R2 is H or halogen; R3 is halogen; R4 is halogen or CH3; and R5 is halogen, cyano, CH3 or C1-C2 alkoxy; and (b) at least one additional fungicidal compound selected from those disclosed herein. Also disclosed is a method for controlling plant diseases caused by fungal plant pathogens comprising applying to the plant or portion thereof, or to the plant seed, a fungicidally effective amount of the aforesaid composition.
• [EN] ANTICANCER COMPOUNDS AND PROCESS FOR THE PREPARATION THEREOF<br/>[FR] COMPOSÉS ANTICANCÉREUX ET PROCÉDÉ DE LEUR PRÉPARATION
  申请人：COUNCIL SCIENT IND RES

  公开号：WO2014128723A2

  公开（公告）日：2014-08-28

  The invention disclosed herein relates to novel Peribysin E analogues of general formula-I. Further the invention provides simple, economical and short synthesis of Peribysin E and its analogues of Formula I, in good yield and purity leading to the identification of more potent cell adhesion inhibitors.