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linoleic acid | 4906-90-5

中文名称
——
中文别名
——
英文名称
linoleic acid
英文别名
8,11-Octadecadiensaeure;cis,cis-8,11-Octadiensaeure;8Z,11Z-octadecadienoic acid;(8Z,11Z)-octadeca-8,11-dienoic acid
linoleic acid化学式
CAS
4906-90-5
化学式
C18H32O2
mdl
——
分子量
280.451
InChiKey
WBTBKRBXTLZUJG-NQLNTKRDSA-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

  • 熔点:
    -16--15.5 °C
  • 沸点:
    407.4±24.0 °C(Predicted)
  • 密度:
    0.911±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    6.8
  • 重原子数:
    20
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.72
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

SDS

SDS:5398ed00d3f9599de75dc0f0f72357ad
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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:
    linoleic acid 作用下, 以 Petroleum ether 为溶剂, 生成
    参考文献:
    名称:
    Synthesis of Unsaturated Fatty Acids. Positional Isomers of Linoleic Acid1
    摘要:
    DOI:
    10.1021/jo01040a023
  • 作为产物:
    描述:
    1,6-二氯己烷二异丁基氢化铝 、 sodium iodide 作用下, 以 乙醚正庚烷 为溶剂, 生成 linoleic acid
    参考文献:
    名称:
    Synthesis of Unsaturated Fatty Acids. Positional Isomers of Linoleic Acid1
    摘要:
    DOI:
    10.1021/jo01040a023
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文献信息

  • Tripod-like Cationic Lipids as Novel Gene Carriers
    作者:Asier Unciti-Broceta、Emma Holder、Lisa J. Jones、Barbara Stevenson、Andrew R. Turner、David J. Porteous、A. Chris Boyd、Mark Bradley
    DOI:10.1021/jm701493f
    日期:2008.7.1
    An innovative family of tridentate-cationic "single-chained lipids" designed to enhance DNA compaction and to promote endosomal escape was synthesized by coupling various lipids to a multibranched scaffold. DNA retardation assays confirmed the ability of the most members of the library to complex DNA. Classical molecular dynamics simulations performed on the lauryl derivative, bound to a short strand of DNA in aqueous solution supported these observations. These showed that two "arms" of the tripodal molecule are ideally suited to forming strong Coulombic interactions with two contiguous phosphate groups from the DNA backbone while the lipophilic tail stays perpendicular to the DNA helix. Gene transfer abilities of the library were assessed in multiple cell lines (CHO, Cos7, and 16HBE14o-) with some library members giving excellent transfection abilities and low cytotoxicity, supporting the use of this tripodal approach for the development of efficient gene delivery agents.
  • (17-ß)-3-OXOANDROST-4-EN-17-YL UNDECANOATE COMPOSITIONS AND METHODS OF THEIR PREPARATION AND USE
    申请人:Lipocine Inc.
    公开号:US20160193225A1
    公开(公告)日:2016-07-07
    Disclosed herein are compositions having a lipophilic active agent and methods of their use.
  • PHARMACEUTICAL COMPOSITION AND METHODS
    申请人:Lipocine Inc.
    公开号:US20160184324A1
    公开(公告)日:2016-06-30
    Disclosed herein are compositions having a lipophilic active agent and methods of their use.
  • (17-ß)-3-Oxoandrost-4-En-17-Yl Undecanoate Compositions and Methods of Their Preparation and Use
    申请人:Lipocine Inc.
    公开号:US20180104257A1
    公开(公告)日:2018-04-19
    Disclosed herein are compositions having a lipophilic active agent and methods of their use.
  • Synthesis of Unsaturated Fatty Acids. Positional Isomers of Linoleic Acid<sup>1</sup>
    作者:Walter J. Gensler、John J. Bruno
    DOI:10.1021/jo01040a023
    日期:1963.5
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