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4'-乙氧基-3'-(三氟甲基)乙酰苯 | 851263-13-3

中文名称
4'-乙氧基-3'-(三氟甲基)乙酰苯
中文别名
——
英文名称
1-[4-ethoxy-3-(trifluoromethyl)phenyl]ethanone
英文别名
4'-Ethoxy-3'-(trifluoromethyl)acetophenone
4'-乙氧基-3'-(三氟甲基)乙酰苯化学式
CAS
851263-13-3
化学式
C11H11F3O2
mdl
——
分子量
232.202
InChiKey
KWNZFVILRICPQN-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:
    276.4±40.0 °C(Predicted)
  • 密度:
    1.190±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.8
  • 重原子数:
    16
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:30637acae51f5757e679e1dabf5436fa
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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

反应信息

  • 作为产物:
    描述:
    4'-氟-3'-(三氟甲基)苯乙酮potassium ethoxide 作用下, 以 乙醇 为溶剂, 反应 2.0h, 以98%的产率得到4'-乙氧基-3'-(三氟甲基)乙酰苯
    参考文献:
    名称:
    Pyrrazolo-pyrimidine derivatives
    摘要:
    本发明涉及式(I)的吡唑并嘧啶衍生物:其中R1至R4和A如说明书中所定义,其制备方法,用于治疗或预防代谢型谷氨酸受体介导的疾病,用于制备治疗此类疾病的药物,以及含有这些衍生物的药物组合物。
    公开号:
    US20060183756A1
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文献信息

  • [EN] PYRAZOLO AND IMIDAZO-PYRIMIDINE DERIVATIVES<br/>[FR] DERIVES DE PYRAZOLO-PYRIMIDINE ET D'IMIDAZO-PYRIMIDINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2005040171A1
    公开(公告)日:2005-05-06
    The present invention relates to novel pyrazolo- and imidazo-pyrimidine derivatives of formula (I) wherein A, D, E, L, M, Q, R1, R2 and R3 are as defined in the description and claims and to processes for their preparation, pharmaceutical compositions containing said derivatives and their use in the prevention and treatment of diseases.
    本发明涉及公式(I)中的新型吡唑啉和咪唑嘧啶生物,其中A、D、E、L、M、Q、R1、R2和R3如描述和索赔中所定义,并涉及其制备方法、含有所述衍生物的药物组合物以及它们在预防和治疗疾病中的用途。
  • 2-아실아미노티아졸 유도체 또는 그의 염
    申请人:Astellas Pharma Inc. 아스텔라스세이야쿠 가부시키가이샤(519980962516)
    公开号:KR20150120516A
    公开(公告)日:2015-10-27
    본 발명자들은, 피라진-2-카르보닐아미노가 2위치에 치환된 티아졸 유도체가 우수한 무스카린 M 수용체 포지티브 알로스테릭 모듈레이터이며, 무스카린 M 수용체에 의한 방광 수축이 관여하는 방광・요로계 질환의 예방 및/또는 치료제로서 유용한 것을 지견해서 본 발명을 완성하였다. 본 발명의 2-아실아미노티아졸 유도체 또는 그의 염은, 무스카린 M 수용체에 의한 방광 수축이 관여하는 방광・요로계 질환, 예를 들어 저활동 방광 등의 배뇨 장애의 예방 및/또는 치료제로서 사용할 수 있다. (식 중, R은, -N(-R)(-R), 또는 치환될 수도 있는 환상 아미노, R은, C 알킬, R는, 치환될 수도 있는 C 알킬, 또는 치환될 수도 있는 C 시클로알킬, R는, 치환될 수도 있는 아릴, 치환될 수도 있는 단환식 방향족 헤테로환, 또는 치환될 수도 있는 2환식 방향족 헤테로환, R은, -H, -OH, -O-(C 알킬), 또는 할로겐)
    这是一段关于一种药物的描述,主要涉及到对膀胱和泌尿系统疾病的预防和治疗。
  • Novel compounds as metabotropic glutamate receptor antagonists
    申请人:McArthur Gatti Silvia
    公开号:US20070072879A1
    公开(公告)日:2007-03-29
    The present invention relates to compounds of formula (I) wherein A, E G, J, L, M, R 1 , R 2 , and R 3 are as defined in the specification and claims. The invention also relates to pharmaceutical compositions containing such compounds and methods for preparing the compounds and compositions. The compounds are metabotropic glutamate receptor antagonists and are useful for the treatment of a variety of CNS disorders.
    本发明涉及具有以下结构的化合物(I)其中A、E、G、J、L、M、R1、R2和R3如规范和索赔中所定义。该发明还涉及含有这种化合物的药物组合物以及制备这些化合物和组合物的方法。这些化合物是代谢型谷酸受体拮抗剂,可用于治疗各种中枢神经系统疾病。
  • [EN] PYRRAZOLO-PYRIMIDINE DERIVATIVES<br/>[FR] DERIVES DE PYRRAZOLO-PYRIMIDINE
    申请人:HOFFMANN LA ROCHE
    公开号:WO2005123738A1
    公开(公告)日:2005-12-29
    The invention relates to compounds of formula (I) wherein R1, R2, R3, R4, R5 and p are as defined in the description and claims as well as to pharmaceutically acceptable salts thereof per se and as pharmaceutically active substances, their manufacture, medicaments based on a compound in accordance with the invention and their production, as well as the use of the compounds in accordance with the invention in the control or prevention of illnesses of the aforementioned kind, and, respectively, for the production of corresponding medicaments.
    该发明涉及公式(I)中R1、R2、R3、R4、R5和p的化合物,其中这些参数在说明和权利要求中有定义,以及其药学上可接受的盐本身和作为药用活性物质,其制备方法,基于与该发明相符合的化合物的药物,以及它们的生产,以及在控制或预防上述疾病方面使用与该发明相符合的化合物,以及分别用于生产相应的药物。
  • Pyrazolo-pyridine
    申请人:Wichmann Juergen
    公开号:US20050130992A1
    公开(公告)日:2005-06-16
    The present invention relates to novel pyrazolo- and imidazo-pyrimidine derivatives of formula I wherein A, D, E, L, M, Q, R 1 , R 2 and R 3 are as defined hereinabove. The present invention also relates to a process for their preparation, a pharmaceutical composition containing said derivatives and a method of treating or preventing acute or chronic neurological disorder comprising administering to a patient in need of such treatment a pharmaceutical composition comprising a therapeutically effective amount of at least one such derivatives. These disorders include acute and chronic disorders
    本发明涉及式I的新型吡唑咪唑嘧啶生物,其中A、D、E、L、M、Q、R1、R2和R3如上所定义。本发明还涉及它们的制备方法,含有该衍生物的药物组合物以及治疗或预防急性或慢性神经障碍的方法,包括向需要该治疗的患者给予含有至少一种该类衍生物的治疗剂量的药物组合物。这些障碍包括急性和慢性障碍。
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