(-)-(R)-13-Hydroxytetradecansaeure-methylester | 88785-26-6

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: (-)-(R)-13-Hydroxytetradecansaeure-methylester
• 英文别名: R-13-hydroxytetradecanoic acid methyl ester；methyl (13R)-13-hydroxytetradecanoate
• CAS: 88785-26-6
• 化学式: C₁₅H₃₀O₃
• 分子量: 258.401
• InChiKey: YRNFMRNZKAELNA-CQSZACIVSA-N

物化性质

• 熔点：
  34-35 °C
• 沸点：
  125 °C(Press: 0.002 Torr)
• 密度：
  0.931±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.7
• 重原子数：
  18
• 可旋转键数：
  13
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.93
• 拓扑面积：
  46.5
• 氢给体数：
  1
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  苯甲酰氯 、 (-)-(R)-13-Hydroxytetradecansaeure-methylester 在 吡啶 作用下， 以 二氯甲烷 为溶剂， 反应 3.0h， 生成
  参考文献：
  名称：

  Products of Cytochrome P450_BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids

  摘要：

  [GRAPHICS]Oxidation of tetradecanoic and hexadecanoic acids by cytochrome P450(Biol) (CYP107H1) produces mainly the 11-, 12-, and 13-hydroxy C-14 fatty acids and the 11- to 15-hydroxy C-16 fatty acids, respectively. In contrast to previous reports, terminal hydroxylation is not observed. The enantiospecificity of fatty acid hydroxylation by P450(Biol) was also determined, and the enzyme was shown to be moderately selective for production of the (R)-alcohols.

  DOI：

  10.1021/ol035254e
• 作为产物：
  描述：

  10-十一烯-1-醇 在 palladium on activated charcoal 、 (S,S)-[N,N-bis(3,5-di-tert-butylsalicylidene)-1,2-cyclohexane-diamino]cobalt(III) acetate 三乙烯二胺 、 咪唑 、 lithium aluminium tetrahydride 、 正丁基锂 、 air 、 氢气 、 tetra(tert-butyl)ammonium iodide 、 sodium hydride 、 溶剂黄146 、 间氯过氧苯甲酸 作用下， 以 四氢呋喃 、 乙醇 、 正己烷 、 二氯甲烷 、 水 、 甲苯 、 乙腈 为溶剂， 20.0 ℃ 、101.33 kPa 条件下， 反应 47.0h， 生成 (-)-(R)-13-Hydroxytetradecansaeure-methylester
  参考文献：
  名称：

  Products of Cytochrome P450_BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids

  摘要：

  [GRAPHICS]Oxidation of tetradecanoic and hexadecanoic acids by cytochrome P450(Biol) (CYP107H1) produces mainly the 11-, 12-, and 13-hydroxy C-14 fatty acids and the 11- to 15-hydroxy C-16 fatty acids, respectively. In contrast to previous reports, terminal hydroxylation is not observed. The enantiospecificity of fatty acid hydroxylation by P450(Biol) was also determined, and the enzyme was shown to be moderately selective for production of the (R)-alcohols.

  DOI：

  10.1021/ol035254e

文献信息

• Kuechler, Birgit; Voss, Gundula; Gerlach, Hans, Liebigs Annalen der Chemie, 1991, # 6, p. 545 - 552
  作者：Kuechler, Birgit、Voss, Gundula、Gerlach, Hans

  DOI：——

  日期：——
• KUCHLER, BIRGIT;VOSS. , GUNDULA;GERLACH, HANS, LIEBIGS ANN. CHEM.,(1991) N, C. 545-552
  作者：KUCHLER, BIRGIT、VOSS. , GUNDULA、GERLACH, HANS

  DOI：——

  日期：——
• VOSS, G.;GERLACH, H., HELV. CHIM. ACTA, 1983, 66, N 7, 2294-2307
  作者：VOSS, G.、GERLACH, H.

  DOI：——

  日期：——
• Products of Cytochrome P450_BioI (CYP107H1)-Catalyzed Oxidation of Fatty Acids
  作者：Max J. Cryle、Nick J. Matovic、James J. De Voss

  DOI：10.1021/ol035254e

  日期：2003.9.1

  [GRAPHICS]Oxidation of tetradecanoic and hexadecanoic acids by cytochrome P450(Biol) (CYP107H1) produces mainly the 11-, 12-, and 13-hydroxy C-14 fatty acids and the 11- to 15-hydroxy C-16 fatty acids, respectively. In contrast to previous reports, terminal hydroxylation is not observed. The enantiospecificity of fatty acid hydroxylation by P450(Biol) was also determined, and the enzyme was shown to be moderately selective for production of the (R)-alcohols.