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Sodium; 10-fluoro-decanoate | 63977-34-4

中文名称
——
中文别名
——
英文名称
Sodium; 10-fluoro-decanoate
英文别名
Decanoic acid, 10-fluoro-, sodium salt;sodium;10-fluorodecanoate
Sodium; 10-fluoro-decanoate化学式
CAS
63977-34-4
化学式
C10H18FO2*Na
mdl
——
分子量
212.24
InChiKey
RXYIFNCNTGFNBO-UHFFFAOYSA-M
BEILSTEIN
——
EINECS
——
  • 物化性质
  • 计算性质
  • ADMET
  • 安全信息
  • SDS
  • 制备方法与用途
  • 上下游信息
  • 反应信息
  • 文献信息
  • 表征谱图
  • 同类化合物
  • 相关功能分类
  • 相关结构分类

计算性质

  • 辛醇/水分配系数(LogP):
    -1.17
  • 重原子数:
    14
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    40.1
  • 氢给体数:
    0
  • 氢受体数:
    3

反应信息

  • 作为产物:
    参考文献:
    名称:
    Evidence for an octanoate synthase operating during the biosynthesis of piliformic acid in Poronia piliformis
    摘要:
    Sodium [1-C-13]-octanoate is incorporated intact into the C-8 unit of piliformic acid 1 in Poronia piliformis whereas sodium [3-C-13]-decanoate 2 is incorporated into this unit only after prior beta-oxidation to [1-C-13]-acetyl-CoA. Also 8-fluoraoctanaote 3 is utilised by P. piliformis as an intact unit to generate 9-fluoropiliformic acid 5 whereas 10-fluorodecanoate 4 is not. These results suggest that octanoate is biosynthesised de novo for secondary metabolism and is not assimilated from higher fatty acids by beta-oxidation. (C) 1998 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0040-4039(98)00102-6
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文献信息

  • Evidence for an octanoate synthase operating during the biosynthesis of piliformic acid in Poronia piliformis
    作者:Helen Culceth、Jens Fuchser、Steven J Moss、Jens Nieschalk、David O'Hagan
    DOI:10.1016/s0040-4039(98)00102-6
    日期:1998.4
    Sodium [1-C-13]-octanoate is incorporated intact into the C-8 unit of piliformic acid 1 in Poronia piliformis whereas sodium [3-C-13]-decanoate 2 is incorporated into this unit only after prior beta-oxidation to [1-C-13]-acetyl-CoA. Also 8-fluoraoctanaote 3 is utilised by P. piliformis as an intact unit to generate 9-fluoropiliformic acid 5 whereas 10-fluorodecanoate 4 is not. These results suggest that octanoate is biosynthesised de novo for secondary metabolism and is not assimilated from higher fatty acids by beta-oxidation. (C) 1998 Elsevier Science Ltd. All rights reserved.
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