摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

1-13C-isoquinoline

中文名称
——
中文别名
——
英文名称
1-13C-isoquinoline
英文别名
isoquinoline
1-13C-isoquinoline化学式
CAS
——
化学式
C9H7N
mdl
——
分子量
130.15
InChiKey
AWJUIBRHMBBTKR-CDYZYAPPSA-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):
    2.1
  • 重原子数:
    10
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    描述:
    甲酸-13C2-苯乙胺 在 palladium on activated charcoal 环己烯 作用下, 生成 1-13C-isoquinoline
    参考文献:
    名称:
    Unexpected structural integrity of gas phase isoquinoline cations that eliminate HCN
    摘要:
    Abstract13C labelling has been used to study isoquinoline molecular ions undergoing breakdown by HCN elimination in a mass spectrometer. For otherwise stable ions caused to fragment by collisional activation, there is no skeletal rearrangement prior to HCN loss. Of the ions formed by 70 eV electron impact, 69% of those which fragment in the ion source by HCN loss retain their structural integrity, as do 44% of the metastable ions. Of the ions that eliminate HCN without prior arrangement, approximately two‐thirds eliminate C‐1 and one‐third eliminate C‐3. Critical energies are reported for the elimination of HCN from pyridine and isoquinoline molecular ions.
    DOI:
    10.1002/oms.1210180308
点击查看最新优质反应信息

文献信息

  • High-Temperature Rearrangements of 2-Acylisoxazol-5(2H)-ones and Related Oxazoles.
    作者:Adrian D. Clark、Uyen T. Ha、Rolf H. Prager、Jason A. Smith
    DOI:10.1071/ch99075
    日期:——

    2-Acyl-3-arylisoxazol-5(2H)-ones give 2-alkyl(aryl)-4-aryloxazoles in good yields at 540°C under flash vacuum pyrolysis conditions, but at higher temperatures the expected oxazoles are accompanied by increasing amounts of isomeric 2,5-disubstituted oxazoles, as well as anilides and decomposition products of the 2,4-disubstituted oxazole. The rearrangement mechanisms have been studied by the use of 13C labelled substrates and p-substituted 3-arylisoxazolones. The 2,5-disubstituted oxazoles are considered to arise from 1H-azirines, and the anilides from the nitrone ketene isomer of the acylisoxazolone.

    2-酰基-3-芳基异噁唑-5(2H)-酮在 540°C 的闪速真空条件下产生 在 540°C 的闪蒸真空热解条件下,可以得到产率很高的 2-烷基(芳基)-4-芳基噁唑。 但在更高温度下,预期的噁唑会伴随着越来越多的异构体出现。 但在更高温度下,预期的噁唑会伴随着越来越多的异构 2,5-二取代噁唑,以及苯胺和分解物。 以及苯胺和 2,4-二取代噁唑的分解产物。 对重排机理的研究采用了 13C 标记的底物和 对取代的 3-芳基异噁唑酮。2,5-二取代的 噁唑被认为来自 1H-吖嗪,而苯胺则来自腈。 苯胺类则来自酰基异噁唑酮的腈酮烯异构体。
  • Unexpected structural integrity of gas phase isoquinoline cations that eliminate HCN
    作者:Michael A. Baldwin、Jeremy Gilmore、Margaret N. Mruzek
    DOI:10.1002/oms.1210180308
    日期:1983.3
    Abstract13C labelling has been used to study isoquinoline molecular ions undergoing breakdown by HCN elimination in a mass spectrometer. For otherwise stable ions caused to fragment by collisional activation, there is no skeletal rearrangement prior to HCN loss. Of the ions formed by 70 eV electron impact, 69% of those which fragment in the ion source by HCN loss retain their structural integrity, as do 44% of the metastable ions. Of the ions that eliminate HCN without prior arrangement, approximately two‐thirds eliminate C‐1 and one‐third eliminate C‐3. Critical energies are reported for the elimination of HCN from pyridine and isoquinoline molecular ions.
查看更多