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(Z)-11-hexadecenyl trifluoromethyl ketone

中文名称
——
中文别名
——
英文名称
(Z)-11-hexadecenyl trifluoromethyl ketone
英文别名
(Z)-1,1,1-trifluoro-13-octadecen-2-one;(Z)-1,1,1-Trifluoro-13-octadecene-2-one;(Z)-1,1,1-trifluorooctadec-13-en-2-one
(Z)-11-hexadecenyl trifluoromethyl ketone化学式
CAS
——
化学式
C18H31F3O
mdl
——
分子量
320.439
InChiKey
CMVYUUYNWUMURT-WAYWQWQTSA-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

  • 作为反应物:
    描述:
    (Z)-11-hexadecenyl trifluoromethyl ketone 作用下, 以 乙腈 为溶剂, 反应 2.5h, 生成 (Z)-1,1,1-Trifluoro-octadec-13-ene-2,2-diol
    参考文献:
    名称:
    New fluorinated derivatives as esterase inhibitors. Synthesis, hydration and crossed specificity studies
    摘要:
    A variety of new fluorinated chemicals have been prepared for the first time and tested as inhibitors of esterases, one of the main enzymes involved in pheromone catabolism, in two economically important pests, the Egyptian armyworm Spodoptera littoralis (SL) and the Mediterranean corn borer Sesamia nonagrioides (SN). Using the respective major component of the pheromone as substrate, the K-m and V-max of the antennal esterase of both insects resulted to be 5.66 x 10(-4) M and 8.47 x 10(-6) Mmin(-1) for SL and 1.61 x 10(-7) M and 1.25 x 10(-7) Mmin(-1) for SN, pointing out that SN esterase has a higher affinity for its corresponding substrate than SL. In general, the trifluoromethyl ketones (TFMKs) exhibited higher inhibitory potency than the corresponding difluoromethyl ketones (DFMKs) or difluoroaldehydes (DFAs). The compounds appeared to hydrate differently in aqueous solution, the extent of hydration following the order: alpha,alpha-DFMKs
    DOI:
    10.1016/s0968-0896(02)00467-4
  • 作为产物:
    描述:
    (Z)-16-iodohexadec-5-ene 以84%的产率得到
    参考文献:
    名称:
    Villuendas Isabel, Parrilla Alfredo, Guerrero Angel, Tetrahedron, 50 (1994) N 44, S 12673-12684
    摘要:
    DOI:
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文献信息

  • EPR/Spin-trapping study of free radical intermediates in the photolysis of trifluoromethyl ketones with initiators
    作者:Esmeralda Rosa、Angel Guerrero、Mª Pilar Bosch、Luis Julià
    DOI:10.1002/mrc.2566
    日期:2010.3
    detection of the elusive trifluoromethyl radical. In contrast, long-chain TFMKs did not provide clues to prove formation of the trifluoromethyl radical but instead to radicals derived by abstraction of one alpha-methylene proton to the carbonyl. Although TFMKs are quite stable to photodegradation in the absence of initiator, methyl ketone 2b and phenyl ketone 3 produce radicals resulting from abstraction
    首次研究了自由基引发剂存在下三氟甲基酮(TFMKs)1a-1e与非氟化酮2a-2b的光顺磁共振光谱。通过捕获2-甲基-2-亚硝基丙烷(MNP)和2,4,6-三叔丁基亚硝基苯(TTBNB)作为自旋阱,可以识别出酮辐照后产生的瞬态自由基。由于在N和O原子上有矛盾的反应性,因此TTBNB在产生苯胺和硝氧基自旋加合物的这类过程中是一种强大的,特别有用的自旋阱。在叔丁基过氧化物的存在下,短链TFMK(例如1,1,1-三氟丙酮(1d)和六氟丙酮(1e))可检测到难以捉摸的三氟甲基。相比之下,长链TFMK没有提供线索证明三氟甲基自由基的形成,而是提供了通过将一个α-亚甲基质子抽象为羰基而衍生的自由基的线索。尽管在没有引发剂的情况下TFMK对光降解非常稳定,但甲基酮2b和苯基酮3产生的自由基是由γ-氢抽象为羰基而产生的。
  • 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。
  • An efficient and expeditious synthesis of functionalized trifluoromethyl ketones through lithium-iodine exchange reaction
    作者:Isabel Villuendas、Alfredo Parrilla、Angel Guerrero
    DOI:10.1016/s0040-4020(01)89400-x
    日期:1994.1
    long-chain triflouromethyl ketones achieved by metallation of the corresponding iodides in the presence of an equimolar amount of tert-butyllithium, followed by reaction with a fluoroacylating agent. Metallation occurs quantitatively at −78°C and, in contrast to what has been generally recommended, there is no need to add the second equivalent of base, since its presence may be detrimental if other electrophilic
    通过在等摩尔量的叔丁基锂存在下将相应的碘化物金属化,然后与氟代酰化剂反应,可以实现长链三氟甲基酮的直接高效合成。金属化在-78°C下定量发生,与通常所建议的相反,不需要添加第二当量的碱,因为如果分子中存在其他亲电子功能,则其存在可能是有害的。
  • Villuendas Isabel, Parrilla Alfredo, Guerrero Angel, Tetrahedron, 50 (1994) N 44, S 12673-12684
    作者:Villuendas Isabel, Parrilla Alfredo, Guerrero Angel
    DOI:——
    日期:——
  • 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.
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