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6,9-Heptadecadiyne | 162152-47-8

中文名称
——
中文别名
——
英文名称
6,9-Heptadecadiyne
英文别名
heptadeca-6,9-diyne
6,9-Heptadecadiyne化学式
CAS
162152-47-8
化学式
C17H28
mdl
——
分子量
232.409
InChiKey
CBUMIRYDOHIOQV-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):
    7.3
  • 重原子数:
    17
  • 可旋转键数:
    8
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.76
  • 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:
    6,9-Heptadecadiyne 在 palladium on barium sulfate 喹啉氢气 作用下, 以 正己烷 为溶剂, 以86%的产率得到(6Z,9Z)-heptadeca-6,9-diene
    参考文献:
    名称:
    Sex attractants of geometrid and noctuid moths: Chemical characterization and field test of monoepoxides of 6,9-dienes and related compounds
    摘要:
    (Z,Z)-6,9-Dienes with straight C-18-C-23 chains were synthesized from linoleic acid, and a C-17 chain was synthesized by hydrogenation of the corresponding 6,9-diyne prepared from propargyl alcohol. Oxidation of the homoconjugated dienes with m-chloroperoxybenzoic acid yielded a 1:1 mixture of two monoepoxides that could be separated by repeated medium-pressure liquid chromatography with a Lobar column. The chemical structure of each positional isomer was confirmed by analyses of the ozonolysis products, and the isomers showed characteristic C-13 signals in their NMR spectra and fragment ions in their EI mass spectra. In addition to the (Z,Z,Z)-3,6,9-trienes with straight C-18-C-23 chains and their monoepoxides, field tests using single source lures incorporating one of the above seven dienes and 14 monoepoxymonoenes were carried out in a forest in Tokyo from 1992 to 1994. Consequently, attraction of six geometrid species and five noctuid species was observed for the first time.
    DOI:
    10.1007/bf02036719
  • 作为产物:
    描述:
    2-癸炔-1-醇三乙胺copper(l) chloride 、 lithium bromide 作用下, 以 四氢呋喃二氯甲烷 为溶剂, 生成 6,9-Heptadecadiyne
    参考文献:
    名称:
    Sex attractants of geometrid and noctuid moths: Chemical characterization and field test of monoepoxides of 6,9-dienes and related compounds
    摘要:
    (Z,Z)-6,9-Dienes with straight C-18-C-23 chains were synthesized from linoleic acid, and a C-17 chain was synthesized by hydrogenation of the corresponding 6,9-diyne prepared from propargyl alcohol. Oxidation of the homoconjugated dienes with m-chloroperoxybenzoic acid yielded a 1:1 mixture of two monoepoxides that could be separated by repeated medium-pressure liquid chromatography with a Lobar column. The chemical structure of each positional isomer was confirmed by analyses of the ozonolysis products, and the isomers showed characteristic C-13 signals in their NMR spectra and fragment ions in their EI mass spectra. In addition to the (Z,Z,Z)-3,6,9-trienes with straight C-18-C-23 chains and their monoepoxides, field tests using single source lures incorporating one of the above seven dienes and 14 monoepoxymonoenes were carried out in a forest in Tokyo from 1992 to 1994. Consequently, attraction of six geometrid species and five noctuid species was observed for the first time.
    DOI:
    10.1007/bf02036719
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文献信息

  • Sex attractants of geometrid and noctuid moths: Chemical characterization and field test of monoepoxides of 6,9-dienes and related compounds
    作者:Tetsu Ando、Hideki Kishi、Naoko Akashio、Xu-Rong Qin、Namiko Saito、Hiroshi Abe、Satoshi Hashimoto
    DOI:10.1007/bf02036719
    日期:1995.3
    (Z,Z)-6,9-Dienes with straight C-18-C-23 chains were synthesized from linoleic acid, and a C-17 chain was synthesized by hydrogenation of the corresponding 6,9-diyne prepared from propargyl alcohol. Oxidation of the homoconjugated dienes with m-chloroperoxybenzoic acid yielded a 1:1 mixture of two monoepoxides that could be separated by repeated medium-pressure liquid chromatography with a Lobar column. The chemical structure of each positional isomer was confirmed by analyses of the ozonolysis products, and the isomers showed characteristic C-13 signals in their NMR spectra and fragment ions in their EI mass spectra. In addition to the (Z,Z,Z)-3,6,9-trienes with straight C-18-C-23 chains and their monoepoxides, field tests using single source lures incorporating one of the above seven dienes and 14 monoepoxymonoenes were carried out in a forest in Tokyo from 1992 to 1994. Consequently, attraction of six geometrid species and five noctuid species was observed for the first time.
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