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2-allyl-6-propoxy phenol | 1005005-55-9

中文名称
——
中文别名
——
英文名称
2-allyl-6-propoxy phenol
英文别名
2-Prop-2-enyl-6-propoxyphenol
2-allyl-6-propoxy phenol化学式
CAS
1005005-55-9
化学式
C12H16O2
mdl
——
分子量
192.258
InChiKey
CRZKZBLQHQIXFL-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):
    3.5
  • 重原子数:
    14
  • 可旋转键数:
    5
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    29.5
  • 氢给体数:
    1
  • 氢受体数:
    2

反应信息

  • 作为产物:
    描述:
    邻丙氧基苯酚potassium carbonate 作用下, 以 丙酮 为溶剂, 反应 10.0h, 生成 2-allyl-6-propoxy phenol
    参考文献:
    名称:
    反对白菜弯角线虫Trichoplusia ni的二烷氧基苯和二烷氧基烯丙基苯的摄食和产卵抑制剂:潜在的昆虫行为控制剂
    摘要:
    在实验室生物测定中,针对白菜弯角曲霉Trichoplusia ni评估了各个二烷氧基苯化合物/对以及通过取代的烯丙氧基苯的克莱森重排获得的羟基或烷氧基取代的烯丙基苯的拒食剂,产卵抑制物和毒性作用。大多数化合物/组强烈抑制幼虫摄食,有些还表现出温和的毒性和产卵抑制作用。一些化合物/组比商业驱虫剂DEET(N,N- diethyl- m-甲苯胺),因为进食和产卵都可以阻止白菜弯角。根据获得的产卵数据,提出了有关产卵部位的一般假设:一种与苯环同一侧的烷基和烯丙基结合的方式会产生阻吓作用,另一种与烷基和烯丙基的结合方式相反。苯环导致刺激。结果表明,某些构效关系对提高化合物的功效和设计用于农业的新型无毒昆虫控制剂很有用。
    DOI:
    10.1021/jf9045123
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文献信息

  • Agonists and Antagonists of Antennal Responses of Gypsy Moth (Lymantria dispar) to the Pheromone (+)-Disparlure and Other Odorants
    作者:Erika Plettner、Regine Gries
    DOI:10.1021/jf904139e
    日期:2010.3.24
    Insects use the sense of smell to guide many behaviors that are important for their survival. The gypsy moth uses a pheromone to bring females and males together over long distances. Male moth antennae are equipped with innervated sensory hairs that selectively respond to pheromone components and other odors. Host plant odors, in particular, are detected by moths and sometimes cause an enhancement of the antennal and behavioral responses of the moths to their pheromone. Inspired by naturally occurring agonists and antagonists of insect pheromone responses, we have screened, by electroantennogram (EAG) recordings, a collection of compound sets and of individual compounds. We have detected interference of some compounds with the EAG responses of male gypsy moth antennae to the pheromone. We describe three activities: (1) short-term inhibition or enhancement of mixed compound + pheromone plumes, (2) long-term inhibition of pure pheromone plumes following a mixed compound 4-pheromone plume, and (3) inhibition of the recovery phase of mixed compound + pheromone plumes. Long-term inhibition was robust, decayed within 30 s, and correlated with the inhibition of recovery; for both activities clear structure-activity patterns were detected. The commercial repellent N,N-diethyltoluamide (DEET) was included for comparison. The most active and reproducible short-term inhibitor was a mixture of 1-allyl-2,4-dimethoxybenzene and 2-allyl-1,3-dimethoxybenzene. The most active long-term inhibitors were a set of 1-alkoxy-4-propoxybenzenes, DEET, and 1-ethoxy-4-propoxybenzene. DEET was more specific in the olfactory responses it inhibited than 1-ethoxy-4-propoxybenzene, and DEET did not inhibit recovery, whereas 1-ethoxy-4-propoxybenzene did. Target sites for the three activities are discussed.
  • 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.
  • Dialkoxybenzene and Dialkoxyallylbenzene Feeding and Oviposition Deterrents against the Cabbage Looper, Trichoplusia ni: Potential Insect Behavior Control Agents
    作者:Yasmin Akhtar、Yang Yu、Murray B. Isman、Erika Plettner
    DOI:10.1021/jf9045123
    日期:2010.4.28
    Most of the compounds/sets strongly deterred larval feeding, with some exhibiting mild toxic and oviposition deterrent effects as well. Some of the compounds/sets were more active than the commercial insect repellent, DEET (N,N-diethyl-m-toluamide), as both feeding and oviposition deterrents against the cabbage looper. On the basis of the obtained oviposition data a general hypothesis was proposed regarding
    在实验室生物测定中,针对白菜弯角曲霉Trichoplusia ni评估了各个二烷氧基苯化合物/对以及通过取代的烯丙氧基苯的克莱森重排获得的羟基或烷氧基取代的烯丙基苯的拒食剂,产卵抑制物和毒性作用。大多数化合物/组强烈抑制幼虫摄食,有些还表现出温和的毒性和产卵抑制作用。一些化合物/组比商业驱虫剂DEET(N,N- diethyl- m-甲苯胺),因为进食和产卵都可以阻止白菜弯角。根据获得的产卵数据,提出了有关产卵部位的一般假设:一种与苯环同一侧的烷基和烯丙基结合的方式会产生阻吓作用,另一种与烷基和烯丙基的结合方式相反。苯环导致刺激。结果表明,某些构效关系对提高化合物的功效和设计用于农业的新型无毒昆虫控制剂很有用。
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