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(E)-1,1,1-Trifluoro-octadec-13-en-2-one | 166812-75-5

中文名称
——
中文别名
——
英文名称
(E)-1,1,1-Trifluoro-octadec-13-en-2-one
英文别名
1,1,1-Trifluorooctadec-13-en-2-one
(E)-1,1,1-Trifluoro-octadec-13-en-2-one化学式
CAS
166812-75-5
化学式
C18H31F3O
mdl
——
分子量
320.439
InChiKey
CMVYUUYNWUMURT-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):
    8
  • 重原子数:
    22
  • 可旋转键数:
    14
  • 环数:
    0.0
  • sp3杂化的碳原子比例:
    0.83
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    4

反应信息

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文献信息

  • METHODS AND COMPOSITIONS FOR CONTROL OF GYPSY MOTHS, Lymanria dispar
    申请人:Plettner Erika
    公开号:US20100190865A1
    公开(公告)日:2010-07-29
    The invention provides in part dialkoxybenzene and eugenol compounds for controlling infestation by a Lymantria dispar , and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; with the provisos that when R2 is at position 2, R3 if present is at position 3, or when R2 is at to position 3, R3 if present is at positions 2 or 4, or when R2 is at position 4, R3 if present is at position 2; or of Formula II: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; or mixtures thereof.
    该发明部分提供了用于控制以及方法的苯基二甲氧基苯和丁香酚化合物对Lymantria dispar的侵害。这些化合物包括式I的化合物:其中R1可以是甲基、乙基、丙基、正丁基、异戊基(3-甲基丁基)或烯丙基;R2可以在2、3或4位,可以为H、甲基、乙基、丙基、正丁基、异戊基(3-甲基丁基)或烯丙基;R3可以选择性地存在于2、3和4位,为烯丙基;但要注意的是,当R2在2位时,如果R3存在,则在3位,或者当R2在3位时,如果R3存在,则在2或4位,或者当R2在4位时,如果R3存在,则在2位;或者式II的化合物:其中R1可以是甲基、乙基、丙基、正丁基、异戊基(3-甲基丁基)或烯丙基;或它们的混合物。
  • METHODS AND COMPOSITIONS FOR CONTROL OF GYPSY MOTHS, LYMANRIA DISPAR
    申请人:Plettner Erika
    公开号:US20100297059A1
    公开(公告)日:2010-11-25
    The invention provides in part dialkoxybenzene and eugenol compounds for controlling infestation by a Lymantria dispar , and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; with the provisos that when R2 is at position 2, R3 if present is at position 3, or when R2 is at position 3, R3 if present is at positions 2 or 4, or when R2 is at position 4, R3 if present is at position 2; or of Formula II: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; or mixtures thereof.
  • METHODS AND COMPOSITIONS FOR CONTROL OF GYPSY MOTH, Lymantria dispar
    申请人:PLETTNER ERIKA
    公开号:US20130045178A1
    公开(公告)日:2013-02-21
    The invention provides in part dialkoxybenzene and eugenol compounds for controlling infestation by a Lymantria dispar , and methods thereof. The compounds include a compound of Formula I: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; R2 may be at positions 2, 3 or 4 and may be H, methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; and R3 may be optionally present at positions 2, 3 and 4, and is allyl; with the provisos that when R2 is at position 2, R3 if present is at position 3, or when R2 is at position 3, R3 if present is at positions 2 or 4, or when R2 is at position 4, R3 if present is at position 2; or of Formula II: where R1 may be methyl, ethyl, propyl, n-butyl, isopentyl (3-methylbutyl) or allyl; or mixtures thereof.
  • US9497963B2
    申请人:——
    公开号:US9497963B2
    公开(公告)日:2016-11-22
  • A new, practical and efficient sulfone-mediated synthesis of trifluoromethyl ketones from alkyl and alkenyl bromides
    作者:Lourdes Muñoz、Esmeralda Rosa、Ma Pilar Bosch、Angel Guerrero
    DOI:10.1016/j.tetlet.2005.03.106
    日期:2005.5
    We report herein a new and efficient method to prepare trifluoromethyl ketones from the corresponding bromides through sulfones in good yields. (c) 2005 Elsevier Ltd. All rights reserved.
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