(Z)-7-十四碳烯-2-酮 | 146955-45-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 中文名称: (Z)-7-十四碳烯-2-酮
• 英文名称: (Z)-7-tetradecen-2-one
• 英文别名: 7-Tetradecen-2-one, (7Z)-；(Z)-tetradec-7-en-2-one
• CAS: 146955-45-5
• 化学式: C₁₄H₂₆O
• 分子量: 210.36
• InChiKey: ZFQMGOCRWDJUCX-HJWRWDBZSA-N

物化性质

• 沸点：
  310.2±21.0℃ (760 Torr)
• 密度：
  0.840±0.06 g/cm3 (20 ºC 760 Torr)
• 闪点：
  114.3±8.9℃
• LogP：
  5.238 (est)

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  15
• 可旋转键数：
  10
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.79
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  1-甲基苯唑 、 (Z)-7-十四碳烯-2-酮 在 lithium diisopropyl amide 作用下， 以 四氢呋喃 、 正庚烷 、 乙基苯 为溶剂， 反应 1.5h， 以39%的产率得到1-methyl-2-[(Z)-5′-dodecenyl]-4(1H)-quinolone
  参考文献：
  名称：

  Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl-4(1H)-quinolones

  摘要：

  A series of 23 new 1-methyl-2-alkenyl-4(1H)quinolones have been synthesized and evaluated in vitro for their antimycobacterial activities against fast growing species of mycobacteria, such as Mycobacterium fortuitum, M. smegmatis and M. phlei. The compounds displayed good to excellent inhibition of the growth of the mycobacterial test strains with improved antimycobacterial activity compared to the hit compound, evocarpine. The most active compounds, which possessed chain length of 11-13 carbons at position-2 displayed potent inhibitory effects with an MIC value of 1.0 mg/L. In a human diploid embryonic lung cell line, MRC-5 cytotoxicity assay, the alkaloids showed weak to moderate cytotoxic activity. Biological evaluation of these evocarpine analogues on the less pathogenic fast growing strains of mycobacteria showed an interesting antimycobacterial profile and provided significant insight into the structure-activity relationships. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.10.060
• 作为产物：
  描述：

  (5-羧基戊基)三苯基溴化磷 在 sodium hexamethyldisilazane 作用下， 以 四氢呋喃 、 乙醚 为溶剂， 反应 8.0h， 生成 (Z)-7-十四碳烯-2-酮
  参考文献：
  名称：

  Design, synthesis and antimycobacterial activities of 1-methyl-2-alkenyl-4(1H)-quinolones

  摘要：

  A series of 23 new 1-methyl-2-alkenyl-4(1H)quinolones have been synthesized and evaluated in vitro for their antimycobacterial activities against fast growing species of mycobacteria, such as Mycobacterium fortuitum, M. smegmatis and M. phlei. The compounds displayed good to excellent inhibition of the growth of the mycobacterial test strains with improved antimycobacterial activity compared to the hit compound, evocarpine. The most active compounds, which possessed chain length of 11-13 carbons at position-2 displayed potent inhibitory effects with an MIC value of 1.0 mg/L. In a human diploid embryonic lung cell line, MRC-5 cytotoxicity assay, the alkaloids showed weak to moderate cytotoxic activity. Biological evaluation of these evocarpine analogues on the less pathogenic fast growing strains of mycobacteria showed an interesting antimycobacterial profile and provided significant insight into the structure-activity relationships. (C) 2010 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.bmc.2010.10.060

文献信息

• [EN] SUBSTITUTED [1,2,4]TRIAZOLE AND IMIDAZOLE COMPOUNDS<br/>[FR] COMPOSÉS IMIDAZOLE ET TRIAZOLE SUBSTITUÉS EN [1,2,4]
  申请人：BASF SE

  公开号：WO2014095655A1

  公开（公告）日：2014-06-26

  The present invention relates to compounds of the formula (I) wherein the substituents are defined in the description and claims, their preparation and uses of the compounds I.

  本发明涉及公式（I）中取代基的化合物，其中取代基在描述和权利要求中定义，以及化合物I的制备和用途。
• [EN] SUBSTITUTED 2-[PHENOXY-PHENYL]-1-[1,2,4]TRIAZOL-1-YL-ETHANOL COMPOUNDS AND THEIR USE AS FUNGICIDES<br/>[FR] COMPOSÉS DE 2-[PHÉNOXYPHÉNYL]-1-[1,2,4]TRIAZOL-1-YL-ÉTHANOL SUBSTITUÉS ET LEUR UTILISATION COMME FONGICIDES
  申请人：BASF SE

  公开号：WO2014082881A1

  公开（公告）日：2014-06-05

  The present invention relates to substituted 2-[phenoxy-phenyl]-1-[1,2,4]triazol-1-yl-ethanol compounds of formula I as defined in the description,and the N-oxides, and salts thereof, their preparation and intermediates for preparing them. The invention also relates to the use of these compounds for combating harmful fungi and seed coated with at least one such compound and also to compositions comprising at least one such compound.

  本发明涉及如描述中所定义的式I的取代2-[苯氧基-苯基]-1-[1,2,4]三唑-1-基乙醇化合物，以及它们的N-氧化物和盐，它们的制备和用于制备它们的中间体。该发明还涉及利用这些化合物来对抗有害真菌，以及至少包含一种这样的化合物的种子包衣和包含至少一种这样的化合物的组合物。
• [EN] SUBSTITUTED [1,2,4]TRIAZOLE COMPOUNDS AND THEIR USE AS FUNGICIDES<br/>[FR] COMPOSÉS TRIAZOLES SUBSTITUÉS EN [1,2,4] ET LEUR UTILISATION COMME FONGICIDES
  申请人：BASF SE

  公开号：WO2014095548A1

  公开（公告）日：2014-06-26

  The present invention relates to compoundsof the formula (I) wherein the variables are defined in the description and claims, their preparation and uses thereof.

  本发明涉及公式（I）中变量的化合物，其中这些变量在描述和权利要求中有定义，以及它们的制备和用途。
• [EN] SUBSTITUTED [1,2,4] TRIAZOLE COMPOUNDS<br/>[FR] COMPOSÉS DE [1,2,4]TRIAZOLE SUBSTITUÉS
  申请人：BASF SE

  公开号：WO2014082880A1

  公开（公告）日：2014-06-05

  The present invention relates to substituted [1,2,4] triazol compounds of the formula I wherein the substituents are defined in the claims and the description, and the N-oxides and the salts thereof for combating phytopathogenic fungi, and to the use and methods for combating phytopathogenic fungi and to seeds coated with at least one such compound. The invention also relates to processes for preparing these compounds, intermediates, processes for preparing such intermediates, and to compositions comprising at least one compound I.

  本发明涉及式I的取代[1,2,4]三唑化合物，其中取代基在权利要求和描述中定义，以及其N-氧化物和盐，用于对抗植物病原真菌，以及用于对抗植物病原真菌的使用和方法，以及至少包含一种这种化合物的种子包衣。该发明还涉及制备这些化合物的方法，中间体，制备这种中间体的方法，以及包含至少一种化合物I的组合物。
• [EN] SUBSTITUTED [1,2,4]TRIAZOLE AND IMIDAZOLE COMPOUNDS<br/>[FR] COMPOSÉS D'IMIDAZOLE ET DE [1,2,4]-TRIAZOLE SUBSTITUÉS
  申请人：BASF SE

  公开号：WO2015086462A1

  公开（公告）日：2015-06-18

  The present invention relates to compoundsof the formula (I) and the N-oxides and the salts there off or combating phytopathogenic fungi, and to the use and methods for combating phytopathogenic fungi and to seeds coated with at least one such compound. The invention also relates to processes for preparing these compounds, intermediates, processes for preparing such intermediates, and to compositions comprising at least one compound I.

  本发明涉及公式（I）的化合物，以及其N-氧化物和盐，用于对抗植物病原真菌，以及用于对抗植物病原真菌的使用和方法，以及至少涂覆有一种这样的化合物的种子。该发明还涉及制备这些化合物的方法，中间体，制备这种中间体的方法，以及包含至少一种化合物I的组合物。