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3-十二烷基苯甲醛 | 307498-21-1

中文名称
3-十二烷基苯甲醛
中文别名
——
英文名称
3-dodecylbenzaldehyde
英文别名
3-Dodecylbenzaldehyde
3-十二烷基苯甲醛化学式
CAS
307498-21-1
化学式
C19H30O
mdl
——
分子量
274.447
InChiKey
ZZFKTLFANQRCAU-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):
    7.6
  • 重原子数:
    20
  • 可旋转键数:
    12
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.63
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    参考文献:
    名称:
    Syntheses and antifungal activity of pseudomycin side-chain analogues. Part 1
    摘要:
    We have described herein the syntheses of three novel series of aromatic ring containing pseudomycin side-chain analogues. Preliminary biological evaluations of these analogues clearly indicate that it is possible to synthesize rigid pseudomycin sidechain analogues without compromising in vitro antifungal activity. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00423-6
  • 作为产物:
    描述:
    间溴苯甲醛 在 palladium/alumina copper(l) iodide 、 TEA 、 氢气三苯基膦 、 palladium dichloride 作用下, 以 乙酸乙酯乙腈 为溶剂, 生成 3-十二烷基苯甲醛
    参考文献:
    名称:
    Syntheses and antifungal activity of pseudomycin side-chain analogues. Part 1
    摘要:
    We have described herein the syntheses of three novel series of aromatic ring containing pseudomycin side-chain analogues. Preliminary biological evaluations of these analogues clearly indicate that it is possible to synthesize rigid pseudomycin sidechain analogues without compromising in vitro antifungal activity. (C) 2000 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0960-894x(00)00423-6
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文献信息

  • LONG CHAIN BASE SPHINGOSINE KINASE INHIBITORS
    申请人:UNIVERSITY OF VIRGINIA PATENT FOUNDATION
    公开号:US20150210675A1
    公开(公告)日:2015-07-30
    The invention relates to inhibitors of Sphingosine Kinase enzymatic activity, and methods of treating diseases and disorders by administering inhibitors of Sphingosine Kinase enzymatic activity.
    本发明涉及抑制鞘氨醇激酶酶活性的抑制剂,以及通过给予鞘氨醇激酶酶活性抑制剂治疗疾病和疾患的方法。
  • Buckminsterfullerene derivatives bearing a fluoroalkyl group for use in organic photovoltaic cells
    作者:Makoto Karakawa、Takabumi Nagai、Tomomi Irita、Kenji Adachi、Yutaka Ie、Yoshio Aso
    DOI:10.1016/j.jfluchem.2012.09.009
    日期:2012.12
    Six novel fluoroalkylpyrrolidine-substituted [60]fullerene derivatives were synthesized and their ability to perform as new n-type organic photovoltaic materials was evaluated. The fullerene derivatives were soluble in common organic solvents, affording good processability properties for the fabrication of photovoltaic cells, and showed an absorption range and molar extinctions similar to those of 16,6]-phenyl C-61 butyric acid methyl ester. Bulk-heterojunction photovoltaic cells using poly(3-hexylthiophene):fullerene derivative blends as the photovoltaic active layers were fabricated and characterized. The performances of the photovoltaic cells were notably affected by the substituents on the fullerene derivatives. Short fluoroalkyl (C4F9) chains on pyrrolidine-linked phenyl groups were suitable substituents for the photovoltaic materials in the current study. This fullerene derivative bearing a C4F9-phenyl group showed a moderate power conversion efficiency of 0.53% during simulated AM 1.5 G solar irradiation at 100 mW/cm(2). This is so far the first report of the use of fluoroalkyl fullerene derivatives as the active materials in organic photovoltaic cells. (C) 2012 Elsevier B.V. All rights reserved.
  • PSEUDOMYCIN N-ACYL SIDE-CHAIN ANALOGS
    申请人:ELI LILLY AND COMPANY
    公开号:EP1200460A1
    公开(公告)日:2002-05-02
  • US9688668B2
    申请人:——
    公开号:US9688668B2
    公开(公告)日:2017-06-27
  • [EN] PSEUDOMYCIN N-ACYL SIDE-CHAIN ANALOGS<br/>[FR] ANALOGUES A BASE DE PSEUDOMYCINE A CHAINES LATERALES N-ACYLE
    申请人:LILLY CO ELI
    公开号:WO2001005814A1
    公开(公告)日:2001-01-25
    Semi-synthetic pseudomycin compounds having structure (I) are described which may be useful as antifungal agents or intermediates in the design of antifungal agents.
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同类化合物

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