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1,3,5-Trimethyladamantyl-7-carboxylic acid chloride | 50741-88-3

中文名称
——
中文别名
——
英文名称
1,3,5-Trimethyladamantyl-7-carboxylic acid chloride
英文别名
3,5,7-trimethyl-1-adamantanecarbonyl chloride;3,5,7-trimethyladamantane-1-carbonyl chloride;3,5,7-Trimethyladamantoyl Chloride
1,3,5-Trimethyladamantyl-7-carboxylic acid chloride化学式
CAS
50741-88-3
化学式
C14H21ClO
mdl
——
分子量
240.773
InChiKey
STZWYHYHQQJKOL-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:
    269.6±9.0 °C(Predicted)
  • 密度:
    1.176±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    16
  • 可旋转键数:
    1
  • 环数:
    4.0
  • sp3杂化的碳原子比例:
    0.93
  • 拓扑面积:
    17.1
  • 氢给体数:
    0
  • 氢受体数:
    1

反应信息

点击查看最新优质反应信息

文献信息

  • Bicycloheteroaryl compounds as P2X7 modulators and uses thereof
    申请人:Kelly G. Michael
    公开号:US20060217448A1
    公开(公告)日:2006-09-28
    Bicycloheteroaryl compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.
    公开了具有以下公式代表的Bicycloheteroaryl化合物:这些化合物可以制备为药物组合物,并可用于预防和治疗包括人类在内的哺乳动物的各种疾病,例如疼痛、炎症、创伤性损伤等。
  • [EN] AMINE OR (THIO)AMIDE CONTAINING LXR MODULATORS<br/>[FR] MODULATEURS DE LXR À BASE D'AMINE OU DE (THIO) AMIDE
    申请人:PHENEX FXR GMBH
    公开号:WO2019016269A1
    公开(公告)日:2019-01-24
    The present invention relates to derivatives of formula (I) which bind to the liver X receptor (LXRα and/or LXRβ) and act preferably as inverse agonists of LXR.
    本发明涉及公式(I)的衍生物,其结合到肝X受体(LXRα和/或LXRβ),并且作为LXR的拮抗剂。
  • Antitumor and immunosuppresive 4-carbamoyl imidazolium-5-olate
    申请人:Sumitomo Chemical Company, Limited
    公开号:US04332806A1
    公开(公告)日:1982-06-01
    There are provided compounds of the formula: ##STR1## wherein R is an adamantoyl group substituted with a lower alkyl group, a lower alkoxy group, a hydroxy group, a lower alkanoyloxy group, an aroyloxy group, a halogen atom, an acetamido group, a nitro group, an azide group, a trifluoromethyl group or a phenyl group which may be substituted with a nitro group, a halogen atom, a lower alkyl group or a lower alkoxy group and a process producing them. These compounds are useful as antitumor agents and immunosuppressants.
    提供了以下化合物的化学式:##STR1## 其中R是一个由低烷基基团、低烷氧基团、羟基、低烷酰氧基团、芳酰氧基团、卤素原子、乙酰胺基团、硝基基团、叠氮基团、三氟甲基基团或苯基取代的金刚烷基团,该苯基可能被硝基基团、卤素原子、低烷基基团或低烷氧基团取代,以及生产这些化合物的过程。这些化合物可用作抗肿瘤剂和免疫抑制剂。
  • [EN] ANTI-INFLAMMATORY AGENTS<br/>[FR] AGENTS ANTI-INFLAMMATOIRES
    申请人:UNIV CAMBRIDGE TECH
    公开号:WO2006016152A1
    公开(公告)日:2006-02-16
    The invention provides compounds, compositions and uses of compounds of general formula (I) or pharmaceutically acceptable salts thereof, which are 3-aminocaprolactam derivatives, for the preparation of a medicament intended to treat an inflammatory disorder wherein X is -CO-Y-(R1)n or SO2-Y-(R1)n; and Y is 0 cycloalkyl or polycyloalkyl group (such as an adamantyl, adamantanemethyl, bicyclooctyl, cyclohexyl, cyclopropyl group); or is 0 cycloalkenyl or polycycloalkenyl group.
    本发明提供了通式(I)的化合物、组合物及其药学上可接受的盐的用途,其中X为-CO-Y-(R1)n或SO2-Y-(R1)n;Y为0环烷基或多环烷基(例如,金刚烷基,金刚烷甲基,双环辛基,环己基,环丙基);或为0环烯基或多环烯基。这些化合物是3-氨基己内酯衍生物,用于制备用于治疗炎症性疾病的药物。
  • Bicycloheteroaryl Compounds as P2X7 Modulators and Uses Thereof
    申请人:Kelly G Michael
    公开号:US20080039478A1
    公开(公告)日:2008-02-14
    Bicycloheteroaryl compounds are disclosed that have a formula represented by the following: The compounds may be prepared as pharmaceutical compositions, and may be used for the prevention and treatment of a variety of conditions in mammals including humans, including by way of non-limiting example, pain, inflammation, traumatic injury, and others.
    本文披露了一种具有以下公式表示的Bicycloheteroaryl化合物:这些化合物可以制备为药物组成物,并可用于预防和治疗哺乳动物包括人类的各种疾病,包括但不限于疼痛,炎症,创伤性损伤等。
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