Cyclohexadecyl-trifluoromethanesulfonyloxy-acetic acid benzyl ester | 260056-03-9

• 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: Cyclohexadecyl-trifluoromethanesulfonyloxy-acetic acid benzyl ester
• CAS: 260056-03-9
• 化学式: C₂₆H₃₉F₃O₅S
• 分子量: 520.654
• InChiKey: XSFWFXNMODXYIT-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  7.45
• 重原子数：
  35.0
• 可旋转键数：
  6.0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.73
• 拓扑面积：
  69.67
• 氢给体数：
  0.0
• 氢受体数：
  5.0

反应信息

• 作为反应物：
  描述：

  Cyclohexadecyl-trifluoromethanesulfonyloxy-acetic acid benzyl ester 在 palladium on activated charcoal 2,6-二甲基吡啶 、 氢气 、 碳酸氢钠 、 N,N'-二环己基碳二亚胺 、 三氟乙酸 作用下， 以 乙醇 、 二氯甲烷 、 乙酸乙酯 、 1,2-二氯乙烷 、 乙腈 为溶剂， 生成 (2R,5S)-2-Cyclohexadecyl-5-hydroxymethyl-1,4,5,6-tetrahydro-2H-benzo[e][1,4]diazocin-3-one
  参考文献：
  名称：

  Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 2-alkylated benzolactams

  摘要：

  The size and position of a hydrophobic moiety on a benzolactam skeleton, which reproduces the active conformation and biological activity of teleocidins, play an important role in the appearance of the activity. Compounds with alkyl groups of various sizes and shapes at the 2-position of benzolactam were synthesized. Structure-activity results indicate that a hydrophobic substituent at the C-2 position plays a critical role in the appearance of biological activities, as in the case of substitution at C-9. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00580-6
• 作为产物：
  描述：

  Cyclohexadecyl-hydroxy-acetic acid 在 2,6-二甲基吡啶 、 1,8-二氮杂双环[5.4.0]十一碳-7-烯 作用下， 以 二氯甲烷 、 苯 为溶剂， 生成 Cyclohexadecyl-trifluoromethanesulfonyloxy-acetic acid benzyl ester
  参考文献：
  名称：

  Role of the hydrophobic moiety of tumor promoters. Synthesis and activity of 2-alkylated benzolactams

  摘要：

  The size and position of a hydrophobic moiety on a benzolactam skeleton, which reproduces the active conformation and biological activity of teleocidins, play an important role in the appearance of the activity. Compounds with alkyl groups of various sizes and shapes at the 2-position of benzolactam were synthesized. Structure-activity results indicate that a hydrophobic substituent at the C-2 position plays a critical role in the appearance of biological activities, as in the case of substitution at C-9. (C) 1999 Elsevier Science Ltd. All rights reserved.

  DOI：

  10.1016/s0960-894x(99)00580-6