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(S)-ethyl-9-hydroxydecenoate | 134733-59-8

中文名称
——
中文别名
——
英文名称
(S)-ethyl-9-hydroxydecenoate
英文别名
(S) ethyl (2E)-9-hydroxydecenoate;ethyl (E,9S)-9-hydroxydec-2-enoate
(S)-ethyl-9-hydroxydecenoate化学式
CAS
134733-59-8
化学式
C12H22O3
mdl
——
分子量
214.305
InChiKey
YJUYFBWOMVOGQO-UQSGXBNBSA-N
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):
    2.7
  • 重原子数:
    15
  • 可旋转键数:
    9
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.75
  • 拓扑面积:
    46.5
  • 氢给体数:
    1
  • 氢受体数:
    3

上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    (S)-ethyl-9-hydroxydecenoatesodium hydroxide 作用下, 以 异丙醇 为溶剂, 反应 22.0h, 以80%的产率得到(S,E)-(+)-9-hydroxydec-2E-enoic acid
    参考文献:
    名称:
    Enzyme reactions in apolar solvents. The resolution of branched and unbranched 2-alkanols by porcine pancreatic lipase.
    摘要:
    Straight-chain and branched 2-alkanols were subjected to enzyme catalyzed transesterification in organic solvent using porcine pancreatic lipase, high enantioselectivity being generally observed. The method was applied to the synthesis of (R)-(-)-9-hydroxy-(E)-decenoic acid, a component of the queen bee mandibular gland pheromone.
    DOI:
    10.1016/s0040-4020(01)96905-4
  • 作为产物:
    描述:
    7-hydroxyheptanal4-甲基苯磺酸吡啶 、 sodium hydride 、 pyridinium chlorochromate 作用下, 以 四氢呋喃甲醇乙醚二氯甲烷 为溶剂, 反应 1.0h, 生成 (S)-ethyl-9-hydroxydecenoate
    参考文献:
    名称:
    Chemoenzymatic synthesis of ferrulactone II and (2E)-9-hydroxydecenoic acid
    摘要:
    A novel and divergent synthesis of the title compounds has been developed. The salient features of the synthesis were use of easily accessible starting material, regioselective organometallic reaction and enzymatic derivation of the key synthons.
    DOI:
    10.1016/0957-4166(95)00296-2
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文献信息

  • Novel Carboxylic Acid and Antidepressant Composition Containing the Same as Active Ingredient
    申请人:Yoshimura Hiroyuki
    公开号:US20100184860A1
    公开(公告)日:2010-07-22
    The present invention provides a novel compound and antidepressant composition that can be effectively used for improving depressed mood and depressed state, particularly for depressed mood and depressed state in menopausal women. The compound of the present invention is represented by the following formula (1): wherein R 1 and R 2 are identical or different and represent a hydrogen atom, a hydroxyl group or an acetyloxy group, and n is an integer of 2 to 7, or a pharmaceutically acceptable salt or ester thereof. This compound is used as an active ingredient in the antidepressant composition. Examples of the compound of the invention include (2E)-9,10-dihydroxy-2-decenoic acid, (2Z)-9,10-dihydroxy-2-decenoic acid, (2E)-9-hydroxy-2-decenoic acid, and (2E)-7-acetoxy-2-heptenoic acid.
    本发明提供了一种新型化合物和抗抑郁剂组合物,可有效用于改善抑郁情绪和抑郁状态,特别是用于绝经期妇女的抑郁情绪和抑郁状态。本发明的化合物由以下式(1)表示:其中R1和R2相同或不同,代表氢原子、羟基或乙酰氧基,n为2至7的整数,或其药学上可接受的盐或酯。该化合物作为抗抑郁剂组合物中的活性成分使用。本发明的化合物示例包括(2E)-9,10-二羟基-2-癸烯酸,(2Z)-9,10-二羟基-2-癸烯酸,(2E)-9-羟基-2-癸烯酸和(2E)-7-乙酰氧基-2-庚烯酸。
  • Enzyme reactions in apolar solvents. The resolution of branched and unbranched 2-alkanols by porcine pancreatic lipase.
    作者:Brian Morgani、Allan C. Oehlschlager、Thomas M. Stokes
    DOI:10.1016/s0040-4020(01)96905-4
    日期:1991.1
    Straight-chain and branched 2-alkanols were subjected to enzyme catalyzed transesterification in organic solvent using porcine pancreatic lipase, high enantioselectivity being generally observed. The method was applied to the synthesis of (R)-(-)-9-hydroxy-(E)-decenoic acid, a component of the queen bee mandibular gland pheromone.
  • US8119839B2
    申请人:——
    公开号:US8119839B2
    公开(公告)日:2012-02-21
  • Chemoenzymatic synthesis of ferrulactone II and (2E)-9-hydroxydecenoic acid
    作者:Archana S. Pawar、S. Sankaranarayanan、Subrata Chattopadhyay
    DOI:10.1016/0957-4166(95)00296-2
    日期:1995.9
    A novel and divergent synthesis of the title compounds has been developed. The salient features of the synthesis were use of easily accessible starting material, regioselective organometallic reaction and enzymatic derivation of the key synthons.
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