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(Z)-ethyl 3-methylhelpt-2-enoate | 73516-50-4

中文名称
——
中文别名
——
英文名称
(Z)-ethyl 3-methylhelpt-2-enoate
英文别名
ethyl 3-methylhepta-2,6-dienoate;ethyl (2Z)-3-methylhepta-2,6-dienoate
(Z)-ethyl 3-methylhelpt-2-enoate化学式
CAS
73516-50-4
化学式
C10H16O2
mdl
——
分子量
168.236
InChiKey
OHPWUPYZQFOCEM-HJWRWDBZSA-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

物化性质

  • 沸点:
    226.0±19.0 °C(Predicted)
  • 密度:
    0.906±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.9
  • 重原子数:
    12
  • 可旋转键数:
    6
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.5
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    2

SDS

SDS:21dba8fe5d25c1c7314172418ead2e68
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上下游信息

  • 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:
    (Z)-ethyl 3-methylhelpt-2-enoate 在 lithium hydroxide 作用下, 以 甲醇 为溶剂, 反应 64.0h, 以92%的产率得到(Z)-3-甲基-2,6-庚二烯酸
    参考文献:
    名称:
    Examination of the olefin–olefin ring closing metathesis to prepare Latrunculin B
    摘要:
    Three subunits of the potent actin polymerization inhibitor Latrunculin B were synthesized and assembled using olefin-olefin ring closing metathesis chemistry to close the 14-membered macrocycle, Metathesis reactions of substrates with various remote protecting group patterns were examined and gave 6,7-E-lactones as the preferred products. (C 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.10.144
  • 作为产物:
    描述:
    ethyl hept-6-en-2-ynoate甲基锂copper(l) iodide 作用下, 以 四氢呋喃 为溶剂, 反应 1.0h, 生成 (Z)-ethyl 3-methylhelpt-2-enoate
    参考文献:
    名称:
    Examination of the olefin–olefin ring closing metathesis to prepare Latrunculin B
    摘要:
    Three subunits of the potent actin polymerization inhibitor Latrunculin B were synthesized and assembled using olefin-olefin ring closing metathesis chemistry to close the 14-membered macrocycle, Metathesis reactions of substrates with various remote protecting group patterns were examined and gave 6,7-E-lactones as the preferred products. (C 2008 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.tetlet.2008.10.144
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文献信息

  • Stereoselective Bifurcating-type Radical Cyclization of<i>gem</i>-Dibromocyclopropanes for the Synthesis of Uniquely Fused 5-3-5-Type Tricyclic Compounds
    作者:Yoshinori Nishii、Atsushi Fujiwara、Kazunori Wakasugi、Misao Miki、Kazunori Yanagi、Yoo Tanabe
    DOI:10.1246/cl.2002.30
    日期:2002.1
    Bifurcating radical cyclization of gem-dibromocyclopropane derivatives afforded novel fused 5-3-5 type tricyclic products with high 5-exo-trig and transannular mode.
    gem-二溴环丙烷衍生物的分叉自由基环化提供了具有高5-exo-trig和跨环模式的新型稠合5-3-5型三环产物。
  • A newly-designed PE-supported arsine for efficient and practical catalytic Wittig olefination
    作者:Peng Wang、Chun-Rong Liu、Xiu-Li Sun、Shuai-Shuai Chen、Jun-Fang Li、Zuowei Xie、Yong Tang
    DOI:10.1039/c1cc16747b
    日期:——
    A newly designed PE-supported arsine has been developed as an excellent catalyst for catalytic Wittig-type olefination. Simple ketones, in particular inactive ketones prove to be suitable substrates for the first time. This reaction provides an easy access to di-, tri-, and tetra-substituted olefins in high yield.
    新设计的一种PE支持的胂已被开发为优秀的催化Wittig型烯化催化剂。简单的酮类,尤其是不活跃的酮类,首次证明是合适的底物。这一反应提供了一条简便的途径,以高产率获得二、三、四取代烯烃。
  • LEE, SUSANNA Y.;NIWA, MAHO;SNIDER, BARRY B., J. ORG. CHEM., 53,(1988) N 10, 2356-2360
    作者:LEE, SUSANNA Y.、NIWA, MAHO、SNIDER, BARRY B.
    DOI:——
    日期:——
  • Examination of the olefin–olefin ring closing metathesis to prepare Latrunculin B
    作者:Jin She、John W. Lampe、Alexandra B. Polianski、Paul S. Watson
    DOI:10.1016/j.tetlet.2008.10.144
    日期:2009.1
    Three subunits of the potent actin polymerization inhibitor Latrunculin B were synthesized and assembled using olefin-olefin ring closing metathesis chemistry to close the 14-membered macrocycle, Metathesis reactions of substrates with various remote protecting group patterns were examined and gave 6,7-E-lactones as the preferred products. (C 2008 Elsevier Ltd. All rights reserved.
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