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2-methyl-nonadec-3-yn-2-ol | 479666-15-4

中文名称
——
中文别名
——
英文名称
2-methyl-nonadec-3-yn-2-ol
英文别名
2-Methylnonadec-3-yn-2-ol
2-methyl-nonadec-3-yn-2-ol化学式
CAS
479666-15-4
化学式
C20H38O
mdl
——
分子量
294.521
InChiKey
UFWSNRFTMXHYRS-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

物化性质

  • 沸点:
    266.7±8.0 °C(Predicted)
  • 密度:
    0.867±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    8.2
  • 重原子数:
    21
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.9
  • 拓扑面积:
    20.2
  • 氢给体数:
    1
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    2-methyl-nonadec-3-yn-2-ol 在 sodium hydroxide 作用下, 以 甲苯 为溶剂, 反应 12.0h, 以68%的产率得到1-十七炔
    参考文献:
    名称:
    Synthesis of Natural Polyacetylenes Bearing Furan Rings
    摘要:
    The first total syntheses of four new polyacetylene compounds have been achieved using convergent routes, which involved Cadiot-Chodkiewicz copper-catalyzed cross-coupling reactions to sp-sp centers as the key steps. 19-Furan-2-ylnonadeca-5,7-diynoic acid (1), 19-furan-2-ylnonadeca-5,7-diynoic acid methyl ester (2), 2-pentacosa-7,9-diynylfuran (3), and 21-furan-2-ylhenicosa-14,16-diyn-1-ol (4) were stable and could be readily identified, isolated, and purified in high overall yields.
    DOI:
    10.1021/np9000637
  • 作为产物:
    描述:
    溴代十五烷2-甲基-3-丁炔-2-醇正丁基锂 作用下, 以 四氢呋喃六甲基磷酰三胺正己烷 为溶剂, 以65%的产率得到2-methyl-nonadec-3-yn-2-ol
    参考文献:
    名称:
    Synthesis of Natural Polyacetylenes Bearing Furan Rings
    摘要:
    The first total syntheses of four new polyacetylene compounds have been achieved using convergent routes, which involved Cadiot-Chodkiewicz copper-catalyzed cross-coupling reactions to sp-sp centers as the key steps. 19-Furan-2-ylnonadeca-5,7-diynoic acid (1), 19-furan-2-ylnonadeca-5,7-diynoic acid methyl ester (2), 2-pentacosa-7,9-diynylfuran (3), and 21-furan-2-ylhenicosa-14,16-diyn-1-ol (4) were stable and could be readily identified, isolated, and purified in high overall yields.
    DOI:
    10.1021/np9000637
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文献信息

  • Synthesis of Natural Polyacetylenes Bearing Furan Rings
    作者:Daniela A. Barancelli、Anderson C. Mantovani、Cristiano Jesse、Cristina W. Nogueira、Gilson Zeni
    DOI:10.1021/np9000637
    日期:2009.5.22
    The first total syntheses of four new polyacetylene compounds have been achieved using convergent routes, which involved Cadiot-Chodkiewicz copper-catalyzed cross-coupling reactions to sp-sp centers as the key steps. 19-Furan-2-ylnonadeca-5,7-diynoic acid (1), 19-furan-2-ylnonadeca-5,7-diynoic acid methyl ester (2), 2-pentacosa-7,9-diynylfuran (3), and 21-furan-2-ylhenicosa-14,16-diyn-1-ol (4) were stable and could be readily identified, isolated, and purified in high overall yields.
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