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1-(heptyloxy)-3-methylbenzene | 57792-37-7

中文名称
——
中文别名
——
英文名称
1-(heptyloxy)-3-methylbenzene
英文别名
heptyl-m-tolyl ether;Heptyl-m-tolyl-aether;3-Heptyloxy-toluol;1-m-Tolyloxy-heptan;n-Heptyl-m-tolyl-aether;1-Heptoxy-3-methylbenzene
1-(heptyloxy)-3-methylbenzene化学式
CAS
57792-37-7
化学式
C14H22O
mdl
——
分子量
206.328
InChiKey
MLIYXTVJLFBOAK-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):
    5.5
  • 重原子数:
    15
  • 可旋转键数:
    7
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.57
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

  • 作为反应物:
    描述:
    1-(heptyloxy)-3-methylbenzene6-甲基烟酸甲酯六氟异丙醇重水 、 palladium diacetate 、 silver fluoride 、 (2,4,6-triisopropylbenzoyl)glycine 作用下, 反应 18.0h, 以80%的产率得到
    参考文献:
    名称:
    钯催化芳烃非定向后期 C-H 氘化
    摘要:
    我们描述了钯催化的芳烃非定向后期氘化。关键方面包括使用D 2 O作为方便且容易获得的氘源以及发现含有N-酰基磺酰胺基团的高活性N,N-二齿配体。报道的方案通过可逆的 C-H 激活步骤实现了高度的氘掺入,并具有非凡的官能团耐受性,允许复杂底物的氘化。各种药学相关基序和相关支架的后期同位素标记就是例证。我们预计这种方法以及其他应用将被证明作为药物开发过程和机制研究的有用工具。
    DOI:
    10.1021/jacs.1c08233
  • 作为产物:
    描述:
    参考文献:
    名称:
    Pinette, Justus Liebigs Annalen der Chemie, 1888, vol. 243, p. 32,40
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Copper-catalyzed formation of carbon-heteroatom and carbon-carbon bonds
    申请人:——
    公开号:US20030065187A1
    公开(公告)日:2003-04-03
    The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
    本发明涉及铜催化的碳-杂原子和碳-碳键形成方法。在某些实施例中,本发明涉及铜催化的方法,用于在酰胺或胺基团的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在酰基肼的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在另一些实施例中,本发明涉及铜催化的方法,用于在含氮杂环芳烃(例如吲哚、吡唑和吲哌)的氮原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氮键。在某些实施例中,本发明涉及铜催化的方法,用于在醇的氧原子与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-氧键。本发明还涉及铜催化的方法,用于在包含亲核碳原子的反应物(例如烯醇酸盐或丙二酸盐负离子)与芳基、杂原基或乙烯卤代物或磺酸酯的活化碳之间形成碳-碳键。重要的是,由于催化剂中铜的低成本,本发明的所有方法都相对廉价。
  • Design, synthesis and acaricidal/insecticidal activities of etoxazole analogues
    作者:Yu-xiu Liu、Xing-cun Wei、Yong-qiang Li、Na Yang、Qing-min Wang
    DOI:10.1039/c3nj00032j
    日期:——
    etoxazole analogues and benzoylphenylureas, a series of 2-(2,6-difluorophenyl)-4-(4-substitutedphenyl)-1,3-oxazolines 4a–y were designed and synthesized. It was found that most of these compounds showed excellent acaricidal activities. They gave above 85% mortality at a concentration of 2.5 mg L−1, both for the eggs and larvae of spider mites. Some compounds also showed excellent insecticidal activities
    基于结构-活性关系 乙恶唑设计并合成了一系列的2-(2,6-二氟苯基)-4-(4-取代的苯基)-1,3-恶唑啉4a-y和苯甲酰基苯基脲。发现大多数这些化合物显示出优异的杀螨活性。当浓度为2.5 mg L -1时,它们对蜘蛛螨的卵和幼虫的死亡率都达到85%以上。一些化合物还表现出优异的杀虫活性。2,4-二苯基-1,3-恶唑啉的4-苯基上的取代基的位置和类型对活性有很大影响。2-(2,6-二氟苯基)-4-(2-Cl-4-(4-Cl-苯氧基)苯基)-1,3-恶唑啉(4r)在2.5 mg L -1下表现出100%的杀螨作用,对甜菜夜蛾和小菜蛾的死亡率分别为12.5 mg L -1和65%和93%,几乎与乙恶唑。新发现的结构-活性关系也可能有益于进一步的杀螨剂/杀虫剂开发。
  • [EN] A PROCESS FOR THE PREPARATION OF TRIAZINE INTERMEDIATES AND A PROCESS FOR THE PREPARATION OF UV ABSORBERS THEREOF<br/>[FR] PROCÉDÉ DE PRÉPARATION D'INTERMÉDIAIRES DE TRIAZINE ET PROCÉDÉ DE PRÉPARATION D'ABSORBEURS UV ASSOCIÉS
    申请人:BASF SE
    公开号:WO2020144093A1
    公开(公告)日:2020-07-16
    The presently claimed invention relates to a novel, highly efficient and general process for the preparation of the triazine intermediates and their use in the preparation of UV absorbers.
    目前所声称的发明涉及一种新颖、高效和通用的三嗪中间体制备过程及其在制备紫外线吸收剂中的应用。
  • Copper-catalyzed formation of carbon heteroatom and carbon-carbon bonds
    申请人:Buchwald L. Stephen
    公开号:US20050215794A1
    公开(公告)日:2005-09-29
    The present invention relates to copper-catalyzed carbon-heteroatom and carbon-carbon bond-forming methods. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of an amide or amine moiety and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In additional embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between a nitrogen atom of an acyl hydrazine and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In other embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-nitrogen bond between the nitrogen atom of a nitrogen-containing heteroaromatic, e.g., indole, pyrazole, and indazole, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. In certain embodiments, the present invention relates to copper-catalyzed methods of forming a carbon-oxygen bond between the oxygen atom of an alcohol and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. The present invention also relates to copper-catalyzed methods of forming a carbon-carbon bond between a reactant comprising a nucleophilic carbon atom, e.g., an enolate or malonate anion, and the activated carbon of an aryl, heteroaryl, or vinyl halide or sulfonate. Importantly, all the methods of the present invention are relatively inexpensive to practice due to the low cost of the copper comprised by the catalysts.
    本发明涉及铜催化的碳-杂原子和碳-碳键形成方法。在某些实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和酰胺或胺基团的氮原子之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和酰肼的氮原子之间形成碳-氮键。在其他实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和含氮杂环芳香族化合物(例如吲哚、吡唑和吲唑)的氮原子之间形成碳-氮键。在某些实施例中,本发明涉及铜催化的方法,用于在苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳和醇的氧原子之间形成碳-氧键。本发明还涉及铜催化的方法,用于在包含亲核碳原子(例如烯醇酸根离子或马隆酸根离子)的反应物和苯基、杂环基或乙烯基卤化物或磺酸盐的活性碳之间形成碳-碳键。重要的是,由于催化剂中铜的低成本,本发明的所有方法都相对廉价易行。
  • Roger; Dvolaitzkaya, Recherches, 1937, vol. 1, # 1, p. 13
    作者:Roger、Dvolaitzkaya
    DOI:——
    日期:——
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