摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

5-(4-氯苯基)-3-甲基-1,2,4-恶二唑 | 89804-65-9

中文名称
5-(4-氯苯基)-3-甲基-1,2,4-恶二唑
中文别名
——
英文名称
3-methyl-5-(4-chlorophenyl)-1,2,4-oxadiazole
英文别名
5-(4-Chlorophenyl)-3-methyl-1,2,4-oxadiazole
5-(4-氯苯基)-3-甲基-1,2,4-恶二唑化学式
CAS
89804-65-9
化学式
C9H7ClN2O
mdl
MFCD28166408
分子量
194.62
InChiKey
CTGIPJXADDXHCT-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):
    2.8
  • 重原子数:
    13
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.111
  • 拓扑面积:
    38.9
  • 氢给体数:
    0
  • 氢受体数:
    3

SDS

SDS:07076ad98403d5992446036cc38ea3d7
查看

反应信息

  • 作为产物:
    描述:
    Alpha,4-二氯苯甲醛肟三乙胺三甲氧基磷 作用下, 以 甲醇乙醚 为溶剂, 反应 98.0h, 生成 5-(4-氯苯基)-3-甲基-1,2,4-恶二唑
    参考文献:
    名称:
    腈氧化物与a肟的环加成反应。3,5-二取代的1,2,4-恶二唑-4-氧化物的一般合成。
    摘要:
    腈氧化物与酰胺肟的环加成是合成具有相同或不同取代基的3,5-二取代的1,2,4-恶二唑-4-氧化物的通用方法。产率仅适中,因为通过与伯环加合物的裂解中释放的胺反应并转化了mid胺肟,消耗了等量的一氧化氮。与过量的腈氧化物一起,1,2,4-恶二唑-4-氧化物进行歧化反应,生成亚硝基羰基中间体和1,2,4-恶二唑。
    DOI:
    10.1016/s0040-4020(96)01088-5
点击查看最新优质反应信息

文献信息

  • SUBSTITUTED N-HETEROCYCLYL- AND N-HETEROARYL-TETRAHYDROPYRIMIDINONES AND THE SALTS THEREOF, AND THE USE OF SAME AS HERBICIDAL ACTIVE SUBSTANCES
    申请人:Bayer Aktiengesellschaft
    公开号:US20200390100A1
    公开(公告)日:2020-12-17
    The present invention relates to substituted N-heterocyclyl- and N-heteroaryltetrahydropyrimidinones of the general formula (I) or salts thereof, where the radicals in the general formula (I) correspond to the definitions given in the description, and to the use thereof as herbicides, in particular for controlling broad-leaved weeds and/or weed grasses in crops of useful plants and/or as plant growth regulators for influencing the growth of crops of useful plants.
    本发明涉及通式(I)或其盐的取代N-杂环烷基和N-杂芳基四氢嘧啶酮,其中通式(I)中的基团对应于描述中给出的定义,并将其用作除草剂,特别是用于控制作物中的阔叶杂草和/或杂草草,并/或作为植物生长调节剂,以影响作物的生长。
  • Tetracyclic compounds
    申请人:HUNG David T.
    公开号:US20090239854A1
    公开(公告)日:2009-09-24
    This disclosure relates to new tetracyclic compounds that may be used to modulate a histamine receptor in an individual. The compounds in one embodiment are tetracyclic [4,3-b]indoles. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及新的四环化合物,可用于调节个体中的组胺受体。在一种实施例中,该化合物为四环[4,3-b]吲哚。还提供了包含该化合物的药物组合物,以及使用该化合物进行各种治疗应用的方法,包括治疗认知障碍、精神障碍、神经递质介导的障碍和/或神经元障碍。
  • Phosphodiesterase Inhibitors
    申请人:Palle P. Venkata
    公开号:US20070259874A1
    公开(公告)日:2007-11-08
    The present invention relates to isoxazoline derivatives and their analogues, which can be used as phosphodiesterase (PDE) type IV selective inhibitors. Compounds disclosed herein can be useful in the treatment of AIDS, asthma, arthritis, bronchitis, chronic obstructive pulmonary disease (COPD), psoriasis, allergic rhinitis, shock, atopic dermatitis, Crohn's disease, adult respiratory distress syndrome (ARDS), eosinophilic granuloma, allergic conjunctivitis, osteoarthritis, ulcerative colitis and other inflammatory diseases, especially in humans. Processes for the preparation of disclosed compounds, pharmaceutical compositions containing the disclosed compounds, and their use as PDE type IV selective inhibitors, are provided.
    本发明涉及异噁唑啉生物及其类似物,可用作磷酸二酯酶(PDE)IV型选择性抑制剂。本文所披露的化合物可用于治疗艾滋病、哮喘、关节炎、支气管炎、慢性阻塞性肺疾病(COPD)、屑病、过敏性鼻炎、休克、特应性皮炎、克罗恩病、成人呼吸窘迫综合症(ARDS)、嗜酸性肉芽肿、过敏性结膜炎、骨关节炎、溃疡性结肠炎和其他炎症性疾病,尤其是在人类中。本文提供了所披露的化合物的制备方法、含有所披露的化合物的药物组合物以及它们作为PDE IV型选择性抑制剂的用途。
  • PYRIDO[3,4-B]INDOLES AND METHODS OF USE
    申请人:JAIN Rajendra Parasmal
    公开号:US20110237582A1
    公开(公告)日:2011-09-29
    This disclosure relates to new heterocyclic compounds that may be used to modulate a histamine receptor in an individual. Pyrido[3,4-b]indoles are described, as are pharmaceutical compositions comprising the compounds and methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及新的杂环化合物,可用于调节个体中的组胺受体。描述了吡咯[3,4-b]吲哚,以及包含该化合物的制药组合物和使用该化合物进行多种治疗应用的方法,包括治疗认知障碍、精神障碍、神经递质介导的障碍和/或神经元障碍。
  • PYRIDO[4,3-B]INDOLES CONTAINING RIGID MOIETIES
    申请人:Medivation Technologies, Inc.
    公开号:US20150051218A1
    公开(公告)日:2015-02-19
    This disclosure is directed to pyrido[4,3-b]indoles having rigid moieties. The compounds in one embodiment are pyrido[4,3-b]indoles having an unsaturated hydrocarbon moiety. The compounds in another embodiment are pyrido[4,3-b]indoles having a cycloalkyl, cycloalkenyl or heterocyclyl moiety. Pharmaceutical compositions comprising the compounds are also provided, as are methods of using the compounds in a variety of therapeutic applications, including the treatment of a cognitive disorder, psychotic disorder, neurotransmitter-mediated disorder and/or a neuronal disorder.
    本公开涉及具有刚性基团的吡啶并[4,3-b]吲哚。在一种实施方式中,化合物是具有不饱和碳氢基团的吡啶并[4,3-b]吲哚。在另一种实施方式中,化合物是具有环烷基,环烯基或杂环基团的吡啶并[4,3-b]吲哚。还提供了包含该化合物的制药组合物,以及使用该化合物进行多种治疗应用的方法,包括治疗认知障碍、精神病性障碍、神经递质介导的障碍和/或神经元障碍。
查看更多