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ethyl 11-formylundecanoate | 151271-75-9

中文名称
——
中文别名
——
英文名称
ethyl 11-formylundecanoate
英文别名
ethyl 12-oxododecanoate;12-oxo-dodecanoic acid ethyl ester;12-Oxo-dodecansaeure-aethylester;12-Oxo-laurinsaure-athylester
ethyl 11-formylundecanoate化学式
CAS
151271-75-9
化学式
C14H26O3
mdl
——
分子量
242.359
InChiKey
WVLXAAYOSTYIMM-UHFFFAOYSA-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):
    3.8
  • 重原子数:
    17
  • 可旋转键数:
    13
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.86
  • 拓扑面积:
    43.4
  • 氢给体数:
    0
  • 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:
    ethyl 11-formylundecanoatesodium hexamethyldisilazane 、 sodium hydroxide 作用下, 以 四氢呋喃 为溶剂, 反应 5.0h, 生成 顺式十二烷酸
    参考文献:
    名称:
    Synthesis and Characterization of Novel Acyl-Glycine Inhibitors of GlyT2
    摘要:
    It has been demonstrated previously that the endogenous compound N-arachidonyl-glycine inhibits the glycine transporter GlyT2, stimulates glycinergic neurotransmission, and provides analgesia in animal models of neuropathic and inflammatory pain. However, it is a relatively weak inhibitor with an IC50, of 9 mu M and is subject to oxidation via cyclooxygenase, limiting its therapeutic value. In this paper we describe the synthesis and testing of a novel series of monounsaturated C18 and C16 acyl-glycine molecules as inhibitors of the glycine transporter GIyT2. We demonstrate that they are up to 28 fold more potent that N-arachidonyl-glycine with no activity at the closely related GlyT1 transporter at concentrations up to 30 mu M. This novel class of compounds show considerable promise as a first generation of GIyT2 transport inhibitors.
    DOI:
    10.1021/acschemneuro.7b00105
  • 作为产物:
    描述:
    氧杂环十三烷-2-酮草酰氯硫酸二甲基亚砜 作用下, 以 氯仿 为溶剂, 反应 20.75h, 生成 ethyl 11-formylundecanoate
    参考文献:
    名称:
    DIHYDROOROTIC ACID DEHYDROGENASE INHIBITOR
    摘要:
    公开号:
    EP2857010B1
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文献信息

  • Direct Hydrogenation of Carboxylic Acids to Corresponding Aldehydes Catalyzed by Palladium Complexes
    作者:Kazuhiro Nagayama、Isao Shimizu、Akio Yamamoto
    DOI:10.1246/bcsj.74.1803
    日期:2001.10
    A variety of carboxylic acids can be directly hydrogenated into the corresponding aldehydes in high yields by using homogeneous catalysts such as [Pd(PPh3)4] or combination of Pd(OAc)2 with tertiary phosphines in the presence of an excess amount of 2,2-dimethylpropionic anhydride (pivalic anhydride). As a typical example, octanoic acid can be converted into octanal in 99% yield in 3 h at 80 °C under 3.0 MPa of H2 in acetone in the presence of pivalic anhydride and a catalyst system composed of Pd(OAc)2 + 5P(p-tol)3. Such hydrogenation is widely applicable to various aliphatic, aromatic, and heterocyclic carboxylic acids as well as to di- and tribasic carboxylic acids. The process allows the presence of other functional groups such as ketonic carbonyl, nitrile, and ester groups and even internal C=C bonds. Heterogeneous palladium catalyst such as palladium on carbon also showed some catalytic activities.
    多种羧酸可以通过均相催化剂如 [Pd(PPh3)4] 或在过量的 2,2-二甲基丙酸酐(新戊酸酐)存在下使用 Pd(OAc)2 与三烷基膦的组合直接氢化为相应的醛,产率很高。作为一个典型例子,辛酸可以在新戊酸酐和由 Pd(OAc)2 + 5P(对甲苯基)3 组成的催化系统存在下,在 80°C、3.0 MPa 的氢气压力下于丙酮中3小时内转化为辛醛,产率达 99%。这种氢化方法广泛适用于各种脂肪族、芳香族和杂环羧酸,以及二元和三元羧酸。该过程允许其他功能团如酮羰基、氰基和酯基甚至内部 C=C 键的存在。异相钯催化剂如碳载钯也显示出一定的催化活性。
  • Effect of carbon chain length in acyl coenzyme A on the efficiency of enzymatic transformation of okadaic acid to 7- O -acyl okadaic acid
    作者:Sachie Furumochi、Tatsuya Onoda、Yuko Cho、Haruhiko Fuwa、Makoto Sasaki、Mari Yotsu-Yamashita、Keiichi Konoki
    DOI:10.1016/j.bmcl.2016.05.027
    日期:2016.7
    Saturated fatty acyl CoAs with a carbon chain length of 14, 16 and 18 exhibited higher yields than those with a carbon chain length of 10 or 12. Acyl CoAs with carbon chain lengths from 14 to 18 and containing either a diene unit, an alkyne unit, or an azide unit in the carbon chain were synthesized and shown to provide the corresponding DTX3 with a yield comparable to that of hexadecanoyl CoA. The three
    冈果酸(原鞭毛原鞭毛体物种的产物)在各种双壳类动物中被转化为7- O-酰基OA。在存在来自双壳类动物消化腺的微粒体级分的情况下,结构转化在体外以酶促方式进行。我们一直在使用LC-MS / MS通过检测7- O来鉴定OA转化酶-酰基OA,也称为dinophysistoxin 3(DTX3)。但是,由于OA转化酶是一种膜蛋白,而DTX3的替代测定是必需的,而溶解膜蛋白的表面活性剂会降低LC-MS / MS的灵敏度。本研究研究了饱和脂肪酰基CoA,其碳链长度为10(癸酰基),12(十二烷酰基),14(十四烷酰基),16(十六烷酰基)和18(十八烷酰基)为体外酰化反应的底物。碳链长度为14、16和18的饱和脂肪酰基CoA的收率高于碳链长度为10或12的饱和脂肪酰基CoA。碳链长度为14至18且包含二烯单元,炔烃单元的酰基CoA ,合成或显示出碳链中的叠氮单元或叠氮化物单元,并显示出可提供与十六烷酰
  • [EN] NOVEL GLYCINE TRANSPORT INHIBITORS FOR THE TREATMENT OF PAIN<br/>[FR] NOUVEAUX INHIBITEURS DE TRANSPORT DE GLYCINE POUR LE TRAITEMENT DE LA DOULEUR
    申请人:UNIV SYDNEY
    公开号:WO2018132876A1
    公开(公告)日:2018-07-26
    The present invention relates to novel glycine transport inhibitor compounds and their use for treating pain.
    本发明涉及新型甘氨酸转运抑制剂化合物及其用于治疗疼痛的用途。
  • Photo-Cleavage of Carbon-Carbon Bond of<b><i>α</i></b>-Iodocycloalkanones Giving<b><i>ω</i></b>,<b><i>ω</i></b>-Dialkoxyalkanoic Ester in Alcohol
    作者:Shun-Jun Ji、C. Akira Horiuchi
    DOI:10.1246/bcsj.73.1645
    日期:2000.7
    The irradiation at λ > 300 nm of α-iodocycloalkanones with a high-pressure mercury lamp in alcohols containing a small amount of water afforded the corresponding ω,ω-dialkoxyalkanoic ester (65—88%) by photochemical cleavage of the C(I)-C=O bond at room temperature. In the case of a commercial fluorescent lamp as the irradiating light source, photochemical ring-opening products were also obtained. The irradiation of 2α-iodo-5α- and 4β-iodo-5β-cholestan-3-ones in methanol gave methyl 2,2-dimethoxy-2,3-seco-5α-cholestan-3-oate and methyl 4,4-dimethoxy-3,4-seco-5β-cholestan-3-oate in 78 and 62% yields, respectively. The photochemical behavior of the cleavage reaction of α-iodocycloalkanones is also discussed on the basis of 2-hydroxycycloalkanone as an intermediate.
    在含有少量水的醇中,用高压汞灯在 λ > 300 纳米波长下照射 α-碘环烷酮,可在室温下通过 C(I)-C=O 键的光化学裂解得到相应的 ω,ω- 二烷氧基烷酸酯(65-88%)。在使用商用荧光灯作为照射光源的情况下,也能获得光化学开环产物。在甲醇中辐照 2α-iodo-5α- 和 4β-iodo-5β-cholestan-3- 酮,可得到 2,2-二甲氧基-2,3-seco-5α-胆甾烷-3-酸甲酯和 4,4-二甲氧基-3,4-seco-5β-胆甾烷-3-酸甲酯,收率分别为 78% 和 62%。此外,还以 2-hydroxycycloalkanone 为中间体,讨论了 α-iodocycloalkanones 裂解反应的光化学行为。
  • Liquid polymer catalyst immobilized on polymer-coated silica: application to hydroformylation
    作者:Liang Hong、Eli Ruckenstein
    DOI:10.1039/c39930001486
    日期:——
    α,ω-Bis(diphenylphosphino)-poly(ethylene glycol-400) and its rhodium carbonyl complex have been attached to a poly(2-hydroxyethyl methacrylate) network coating on porous silica; the supported catalytic liquid polymer phase thus obtained has been used in the hydroformylation of ethyl undec-10-enoate.
    α,ω-双(二苯基膦)-聚(乙二醇-400)及其羰基铑络合物被附着到多孔二氧化硅上的聚(2-羟乙基甲基丙烯酸酯)网络涂层上;由此获得的支撑催化液态聚合物相被用于十一-10-烯酸乙酯的氢化甲酰化反应。
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