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(E,E,E,E)-6,10,14,18,22-pentamethyl-1-trimethylsilyltricosa-5,9,13,17,21-pentaen-1-yne | 257885-49-7

中文名称
——
中文别名
——
英文名称
(E,E,E,E)-6,10,14,18,22-pentamethyl-1-trimethylsilyltricosa-5,9,13,17,21-pentaen-1-yne
英文别名
(all-E)-6,10,14,18,22-pentamethyl-1-trimethylsilyl-5,9,13,17,21-tricosapentaen-1-yne;trimethyl-[(5E,9E,13E,17E)-6,10,14,18,22-pentamethyltricosa-5,9,13,17,21-pentaen-1-ynyl]silane
(E,E,E,E)-6,10,14,18,22-pentamethyl-1-trimethylsilyltricosa-5,9,13,17,21-pentaen-1-yne化学式
CAS
257885-49-7
化学式
C31H52Si
mdl
——
分子量
452.839
InChiKey
RARKZGICDZBZEN-HUZMQAKGSA-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:
    509.7±29.0 °C(Predicted)
  • 密度:
    0.860±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    10.52
  • 重原子数:
    32
  • 可旋转键数:
    15
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.61
  • 拓扑面积:
    0
  • 氢给体数:
    0
  • 氢受体数:
    0

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

反应信息

  • 作为反应物:
    描述:
    (E,E,E,E)-6,10,14,18,22-pentamethyl-1-trimethylsilyltricosa-5,9,13,17,21-pentaen-1-yne四丁基氟化铵 作用下, 以 四氢呋喃 为溶剂, 反应 0.5h, 以96%的产率得到(E,E,E,E)-6,10,14,18,22-pentamethyltricosa-5,9,13,17,21-pentaen-1-yne
    参考文献:
    名称:
    A Convergent Approach to Coenzyme Q
    摘要:
    Syntheses of coenzyme Q(3-8) are described, as well as related systems such as plastoquinone-5. Preparation of thr higher homologues of the ubiquinones relies on two new conjunctive reagents, or "linchpins", each of which ultimately corresponds to two or three prenyl units. These allow for attachment of a polyprenyl halide at one end, followed by a Ni(0)-catalyzed cross-coupling at the other terminus with a chloromethylated p-quinone.
    DOI:
    10.1021/ja992164p
  • 作为产物:
    描述:
    (E)-8-iodo-6-methyl-1-trimethylsilyl-5-octen-1-yne 在 叔丁基锂 作用下, 以 乙醚正戊烷 为溶剂, 反应 1.5h, 生成 (E,E,E,E)-6,10,14,18,22-pentamethyl-1-trimethylsilyltricosa-5,9,13,17,21-pentaen-1-yne
    参考文献:
    名称:
    A Novel, Highly Selective, and General Methodology for the Synthesis of 1,5-Diene-Containing Oligoisoprenoids of All Possible Geometrical Combinations Exemplified by an Iterative and Convergent Synthesis of Coenzyme Q10
    摘要:
    GRAPHICSA truly general, versatile, and highly regio- and stereoselective methodology for the synthesis of terpenoids containing 1,5-diene units of E and/or Z geometry critically involves Pd-catalyzed homoallyl- and homopropargyl-alkenyl coupling and Zr-catalyzed carboalumination of alkynes. By using this methodology, coenzyme Q(10), (E,Z,E)-geranylgeranoll, and other natural or unnatural compounds have been synthesized efficiently.
    DOI:
    10.1021/ol010263d
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文献信息

  • A Convergent Approach to Coenzyme Q
    作者:Bruce H. Lipshutz、Gerd Bulow、Fernando Fernandez-Lazaro、Sung-Kyu Kim、Richard Lowe、Paul Mollard、Kirk L. Stevens
    DOI:10.1021/ja992164p
    日期:1999.12.1
    Syntheses of coenzyme Q(3-8) are described, as well as related systems such as plastoquinone-5. Preparation of thr higher homologues of the ubiquinones relies on two new conjunctive reagents, or "linchpins", each of which ultimately corresponds to two or three prenyl units. These allow for attachment of a polyprenyl halide at one end, followed by a Ni(0)-catalyzed cross-coupling at the other terminus with a chloromethylated p-quinone.
  • A Novel, Highly Selective, and General Methodology for the Synthesis of 1,5-Diene-Containing Oligoisoprenoids of All Possible Geometrical Combinations Exemplified by an Iterative and Convergent Synthesis of Coenzyme Q<sub>10</sub>
    作者:Ei-ichi Negishi、Show-Yee Liou、Caiding Xu、Shouquan Huo
    DOI:10.1021/ol010263d
    日期:2002.1.1
    GRAPHICSA truly general, versatile, and highly regio- and stereoselective methodology for the synthesis of terpenoids containing 1,5-diene units of E and/or Z geometry critically involves Pd-catalyzed homoallyl- and homopropargyl-alkenyl coupling and Zr-catalyzed carboalumination of alkynes. By using this methodology, coenzyme Q(10), (E,Z,E)-geranylgeranoll, and other natural or unnatural compounds have been synthesized efficiently.
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