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2-(3,5-bis(trifluoromethyl)benzyloxy)-1-phenylethanone | 345579-46-6

中文名称
——
中文别名
——
英文名称
2-(3,5-bis(trifluoromethyl)benzyloxy)-1-phenylethanone
英文别名
2-{[3,5-Bis(trifluoromethyl)phenyl]methoxy}-1-phenylethan-1-one;2-[[3,5-bis(trifluoromethyl)phenyl]methoxy]-1-phenylethanone
2-(3,5-bis(trifluoromethyl)benzyloxy)-1-phenylethanone化学式
CAS
345579-46-6
化学式
C17H12F6O2
mdl
——
分子量
362.271
InChiKey
FQLPGYFOLQVTLE-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:
    336.0±42.0 °C(Predicted)
  • 密度:
    1.334±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    4.8
  • 重原子数:
    25
  • 可旋转键数:
    5
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.24
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    8

SDS

SDS:ed5a17fbb7b56c2a1aafd22a20da61a1
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上下游信息

  • 上游原料
    中文名称 英文名称 CAS号 化学式 分子量
  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    2-(3,5-bis(trifluoromethyl)benzyloxy)-1-phenylethanone 在 lithium aluminium tetrahydride 、 三乙酰氧基硼氢化钠 、 zinc(II) iodide 作用下, 以 四氢呋喃甲醇乙醚二氯甲烷 为溶剂, 反应 21.0h, 生成
    参考文献:
    名称:
    Cyclic urea derivatives as potent NK1 selective antagonists
    摘要:
    A series of novel five- and six-membered ring urea derivatives have been described as potent and selective NK1 receptor antagonists. Several compounds in this series exhibited good oral activity and brain penetration. Syntheses of these compounds are also described herein. (c) 2005 Elsevier Ltd. All rights reserved.
    DOI:
    10.1016/j.bmcl.2005.05.111
  • 作为产物:
    描述:
    2-(3,5-bis(trifluoromethyl)benzyloxymethyl)-2-phenyl-[1,3]dioxolane盐酸 作用下, 以 四氢呋喃 为溶剂, 反应 20.0h, 以96%的产率得到2-(3,5-bis(trifluoromethyl)benzyloxy)-1-phenylethanone
    参考文献:
    名称:
    WO2006/106727
    摘要:
    公开号:
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文献信息

  • Aryloxyalkylamine NK-1/SSRI inhibitors
    申请人:Huang Yazhong
    公开号:US20060020019A1
    公开(公告)日:2006-01-26
    The invention encompasses compounds of Formula I, including pharmaceutically acceptable salts and solvates, their pharmaceutical compositions, and their use in treating disorders associated with an excess or imbalance of tachykinins or serotonin or both.
    本发明包括式I化合物,包括药物可接受的盐和溶剂化物,它们的药物组合物,以及它们用于治疗与速激肽或血清素或两者过量或不平衡相关的疾病。
  • Benzyloxypropylamine Derivative
    申请人:Higashiura Kunihiko
    公开号:US20080262230A1
    公开(公告)日:2008-10-23
    Disclosed is a novel benzyloxypropylamine derivative having an excellent tachykinin receptor antagonistic effect. This compound shows a good transfer into the blood and a long blood half-life in the blood kinetic test using a guinea pig orally administered with the compound and is stable in an animal plasma. The compound also shows a high transfer to the central nervous system when it is orally administered to a guinea pig at a certain dose. Accordingly, the benzyloxypropylamine derivative is quite useful as a novel anti-tachykinin agent.
    本发明涉及一种新型苄氧基丙胺衍生物,具有优异的缓解速激肽受体拮抗作用。该化合物在豚鼠口服该化合物进行血动力学测试时,表现出良好的转移入血液和长血液半衰期,并在动物血浆中稳定。该化合物还表现出在豚鼠口服一定剂量时,对中枢神经系统的高转移。因此,该苄氧基丙胺衍生物作为一种新型抗速激肽药物非常有用。
  • Benzyloxypropylamine derivative
    申请人:Nippon Zoki Pharmaceutical Co., Ltd.
    公开号:US07939552B2
    公开(公告)日:2011-05-10
    Disclosed is a novel benzyloxypropylamine derivative having an excellent tachykinin receptor antagonistic effect. This compound shows a good transfer into the blood and a long blood half-life in the blood kinetic test using a guinea pig orally administered with the compound and is stable in an animal plasma. The compound also shows a high transfer to the central nervous system when it is orally administered to a guinea pig at a certain dose. Accordingly, the benzyloxypropylamine derivative is quite useful as a novel anti-tachykinin agent.
    本发明公开了一种新型苯甲氧基丙胺衍生物,具有优异的速激肽受体拮抗作用。该化合物在豚鼠口服该化合物后的血液动力学测试中表现出良好的转移进入血液和长血液半衰期,并在动物血浆中稳定。当以一定剂量口服给豚鼠时,该化合物还表现出高转移至中枢神经系统。因此,该苯甲氧基丙胺衍生物作为一种新型抗速激肽药物非常有用。
  • Asymmetric Synthesis of 4,4-Disubstituted-2-Imidazoli-dinones:  Potent NK<sub>1</sub> Antagonists
    作者:Gregory A. Reichard、Carmine Stengone、Sunil Paliwal、Ingrid Mergelsberg、Sapna Majmundar、Cheng Wang、Robert Tiberi、Andrew T. McPhail、John J. Piwinski、Neng-Yang Shih
    DOI:10.1021/ol030104p
    日期:2003.11.1
    A highly efficient and practical synthesis of 4,4-Disubstituted-2-Imidazolidinones utilizing a "self-reproduction of the center of chirality" strategy is described.
  • BENZYLOXYPROPYLAMINE DERIVATIVE
    申请人:NIPPON ZOKI PHARMACEUTICAL CO. LTD.
    公开号:EP1870396B1
    公开(公告)日:2012-10-31
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