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4-allyl-2-methoxy-1-methylbenzene | 40793-85-9

中文名称
——
中文别名
——
英文名称
4-allyl-2-methoxy-1-methylbenzene
英文别名
4-allyl-2-methoxy-phenol;eugenol;5-Allyl-2-methyl-anisol;2-Methoxy-1-methyl-4-prop-2-enylbenzene
4-allyl-2-methoxy-1-methylbenzene化学式
CAS
40793-85-9
化学式
C11H14O
mdl
——
分子量
162.232
InChiKey
YZNOMSLDLDBLTK-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

物化性质

  • 沸点:
    226.4±9.0 °C(Predicted)
  • 密度:
    0.931±0.06 g/cm3(Temp: 20 °C; Press: 760 Torr)(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    3.3
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为产物:
    参考文献:
    名称:
    烯丙基环己二酮的酸催化二烯酮-苯酚重排;电荷诱导和电荷控制的σ反应†
    摘要:
    三氟乙酸和其他布朗斯台德酸催化的10-烯丙基-2-氧代-Δ1 (9),3-六氢萘(12)的重排几乎只产生了[3 s,3 s ]产物1-和3- 5,6,7,8-四氢-2-萘烯丙基(分别为16和15)。用三氟乙酸酐或乙酸酐/硫酸对12进行重排,除15和16外,还会产生可观数量的[1 s,2 s ]重排产物4-烯丙基5,6,7,8-四氢- 2-萘酚(14)(表1)。
    DOI:
    10.1002/hlca.19730560104
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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。
  • Phosphoramidate Derivatives of Nucleosides
    申请人:Centocor Ortho Biotech Products L.P.
    公开号:EP2166016A1
    公开(公告)日:2010-03-24
    Compounds of formula I : R1 is hydrogen, C1-C4alkyl, OH, C1-C4alkoxy; R2 is phenyl, optionally substituted with 1, 2 or 3 substituents each independently selected from halo, C1-C6alkyl, and C1-C6alkoxy, or R2 is naphtalenyl; R3 is hydrogen, C1-C6alkyl, benzyl; R4 is hydrogen, C1-C6alkyl, benzyl; or R3 and R4 together with the carbon atom to which they are attached form C3-C7cycloalkyl; R5 is C1-C6alkyl, benzyl, or phenyl, optionally substituted with 1, 2 or 3 substituents each independently selected from hydroxy, C1-C6alkoxy, amino, mono- and diC1-C6alkylamino; or a pharmaceutically acceptable salt or solvate thereof; useful in the prophylaxis or treatment of HCV infections.
    公式I的化合物:R1是氢、C1-C4烷基、羟基、C1-C4烷氧基;R2是苯基,可选地取代有1、2或3个取代基,每个取代基独立选择自卤素、C1-C6烷基和C1-C6烷氧基,或者R2是萘基;R3是氢、C1-C6烷基、苄基;R4是氢、C1-C6烷基、苄基;或者R3和R4与它们连接的碳原子一起形成C3-C7环烷基;R5是C1-C6烷基、苄基或苯基,可选地取代有1、2或3个取代基,每个取代基独立选择自羟基、C1-C6烷氧基、氨基、单烷基和双烷基氨基;或其药学上可接受的盐或溶剂;用于预防或治疗丙型肝炎感染。
  • Palladium-Catalyzed Regioselective Allylation of Chloromethyl(hetero)arenes with Allyl Pinacolborate
    作者:Sheng Zhang、Aziz Ullah、Yoshinori Yamamoto、Ming Bao
    DOI:10.1002/adsc.201700350
    日期:2017.8.17
    The palladium-catalyzed regioselective allylation reaction between chloromethyl(hetero)arenes and allyl pinacolborate is reported in this work. Chloromethylarenes smoothly reacted with allyl pinacolborate, producing para-allylated dearomatization products or para-allylated arenes in satisfactory to good yields. 2-(Chloromethyl)thiophenes and 2-(chloromethyl)furans bearing substituents on the 5-positions
    在这项工作中报道了氯甲基(杂)芳烃与频哪醇硼酸烯丙酯之间的钯催化的区域选择性烯丙基化反应。氯甲基芳烃与频哪醇硼酸烯丙基酯平稳反应,以令人满意的产率获得对芳基化的脱芳烃化产物或对芳基化的芳烃。在5-位带有取代基的2-(氯甲基)噻吩和2-(氯甲基)呋喃也与频哪醇硼酸烯丙酯平滑地反应,以令人满意的产率产生5-烯丙基化的脱芳香化产物。
  • [EN] USE OF ESTER DERIVATIVE OF TRYPTOPHAN AS DEODORANT AND/OR PERFUME AGENT<br/>[FR] UTILISATION D'UN DÉRIVÉ D'ESTER DE TRYPTOPHANE EN TANT QUE DÉSODORISANT ET/OU PARFUM DE TOILETTE
    申请人:OREAL
    公开号:WO2016097398A1
    公开(公告)日:2016-06-23
    This invention relates to the use of at least one following compound having formula (I), as well as the salts thereof, the optical and geometric isomers thereof, and the solvates thereof, as deodorant agent for treating body odor, preferably underarm odor:
    本发明涉及使用至少一种具有以下化合物(I)的公式,以及其盐,光学和几何异构体以及溶剂合物,作为治疗体味,特别是腋下味的除臭剂:
  • Palladium-Catalyzed sp<sup>2</sup>–sp<sup>3</sup> Coupling of Chloromethylarenes with Allyltrimethoxysilane: Synthesis of Allyl Arenes
    作者:Sheng Zhang、Jinfang Cai、Yoshinori Yamamoto、Ming Bao
    DOI:10.1021/acs.joc.7b00678
    日期:2017.6.2
    Palladium-catalyzed remote sp2–sp3 coupling reaction of chloromethylarenes with allyltrimethoxysilane is described in this work. The allylation reaction regioselectively occurred on the para-positions of 1-(chloromethyl)naphthalenes and benzyl chlorides to form new C(sp2)–C(sp3) bonds. The reaction proceeds smoothly under mild conditions to produce allyl arenes in moderate to excellent yields.
    这项工作描述了氯甲基芳烃与烯丙基三甲氧基硅烷的钯催化的远程sp 2 –sp 3偶联反应。烯丙基化反应区域选择性地发生在1-(氯甲基)萘和苄基氯的对位上,形成新的C(sp 2)–C(sp 3)键。反应在温和条件下平稳进行,以中等至极好的收率生产烯丙基芳烃。
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