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1-(2-ethoxy-4-fluorophenyl)ethanone | 51788-79-5

中文名称
——
中文别名
——
英文名称
1-(2-ethoxy-4-fluorophenyl)ethanone
英文别名
2'-Ethoxy-4'-fluoroacetophenon
1-(2-ethoxy-4-fluorophenyl)ethanone化学式
CAS
51788-79-5
化学式
C10H11FO2
mdl
——
分子量
182.195
InChiKey
SXCHYBKJTBPXQC-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
  • 重原子数:
    13
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.3
  • 拓扑面积:
    26.3
  • 氢给体数:
    0
  • 氢受体数:
    3

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

点击查看最新优质反应信息

文献信息

  • <sup>19</sup>F nuclear magnetic resonance studies of aromatic compounds. Part V. Conformational preferences of side chains in ortho-substituted para-fluoro-acetophenones,-α-methylstyrenes, and -αα-dimethylbenzyl alcohols
    作者:Morris G. Belsham、Andrew R. Muir、Michael Kinns、Lawrence Phillips、Li-Ming Twanmoh
    DOI:10.1039/p29740000119
    日期:——
    shielding of para-fluorine nuclei in the series of acetophenones and α-methylstyrenes named in the title is used to estimate the interplanar angle between the side chain and the ring in the preferred conformations. In the series of dimethylbenzyl alcohols, an analogous torsion angle (between the C–OH bond and the aromatic ring) is defined and estimated. No information is obtainable from the 19F n.m.r. studies
    的屏蔽段在系列中的标题命名为苯乙酮和α甲基苯乙烯的-氟核被用于估计在优选的构象的侧链和环之间的面间角。在二甲基苄醇系列中,定义并估算了类似的扭转角(在C–OH键和芳环之间)。从19 F nmr研究无法获得有关侧链与原取代基之间的顺式或反式关系的信息,因为估算的角度可能对应于两种情况。分析方法利用CNDO / 2 MO计算方法,其中电荷密度分布随每个系列的代表性成员中侧链构象的变化而变化。
  • ANTIPROLIFERATIVE COMPOUNDS AND METHODS OF USE THEREOF
    申请人:Celgene Corporation
    公开号:US20200163948A1
    公开(公告)日:2020-05-28
    Compounds of formula I for treating, preventing or managing cancer are disclosed. Also disclosed are methods of treating, preventing or managing cancer, such as leukemia, comprising administering the compounds. In certain embodiments, the method of treatment comprise administering a compound provided herein in combination with a second agent. Pharmaceutical compositions and single unit dosage forms comprising the compounds are also disclosed.
    本文揭示了化学式I的化合物,用于治疗、预防或管理癌症。还揭示了治疗、预防或管理癌症的方法,例如治疗白血病,包括给予这些化合物。在某些实施例中,治疗方法包括与第二药物联合给药。此外,还揭示了包含这些化合物的药物组合物和单剂量形式。
  • [EN] ANTIPROLIFERATIVE COMPOUNDS AND METHODS OF USE THEREOF<br/>[FR] COMPOSÉS ANTIPROLIFÉRATIFS ET MÉTHODES D'UTILISATION DESDITS COMPOSÉS
    申请人:CELGENE CORP
    公开号:WO2016007848A1
    公开(公告)日:2016-01-14
    Compounds of formula (I) for treating, preventing or managing cancer are disclosed. Also disclosed are methods of treating, preventing or managing cancer, such as leukemia, comprising administering the compounds. In certain embodiments, the method of treatment comprise administering a compound provided herein in combination with a second agent. Pharmaceutical compositions and single unit dosage forms comprising the compounds are also disclosed. In Formula (I) R1 is optionally substituted cycloalkyi, aryl, heteroaryl or heterocyclyl; and R2 and R3 are each halo.
    本发明揭示了化学式(I)的化合物,用于治疗、预防或管理癌症。同时,还揭示了治疗、预防或管理癌症的方法,例如白血病,包括给予该化合物。 在某些实施例中,治疗方法包括联合给予本文提供的化合物和第二药物。还揭示了包含该化合物的制药组合物和单剂量形式。 在化学式(I)中,R1是可选的取代环烷基,芳基,杂芳基或杂环烷基;R2和R3均为卤素。
  • OXAZOLE COMPOUND AND PHARMACEUTICAL COMPOSITION
    申请人:Okada Minoru
    公开号:US20090221586A1
    公开(公告)日:2009-09-03
    The present invention provides a oxazole compound represented by Formula (1), or a salt thereof: wherein R 1 is an aryl group which may have one or more substituents; R 2 is an aryl group or a nitrogen atom-containing heterocyclic group each of which may have one or more substituents; and W is a divalent group represented by —Y 1 -A 1 - or —Y 2 —C(═O)— wherein Y 1 is a group such as —C(═O)—, A 1 is a group such as a lower alkylene group, and Y 2 is a group such as a piperazinediyl group. The oxazole compound has a specific inhibitory action against phosphodiesterase 4.
    本发明提供了一种由公式(1)表示的噁唑化合物或其盐:其中,R1是一个芳基基团,可以具有一个或多个取代基;R2是一个芳基基团或含有氮原子的杂环基团,每个基团都可以具有一个或多个取代基;W是一个由—Y1-A1-或—Y2—C(═O)—表示的二价基团,其中Y1是例如—C(═O)—的基团,A1是例如低碳链基团的基团,而Y2是例如哌嗪二基基团的基团。该噁唑化合物具有特定的磷酸二酯酶4的抑制作用。
  • Antiproliferative compounds and methods of use thereof
    申请人:Celgene Corporation
    公开号:US11241423B2
    公开(公告)日:2022-02-08
    Compounds of formula I for treating, preventing or managing cancer are disclosed. Also disclosed are methods of treating, preventing or managing cancer, such as leukemia, comprising administering the compounds. In certain embodiments, the method of treatment comprise administering a compound provided herein in combination with a second agent. Pharmaceutical compositions and single unit dosage forms comprising the compounds are also disclosed.
    本发明公开了用于治疗、预防或控制癌症的式 I 化合物。还公开了治疗、预防或控制癌症(如白血病)的方法,包括施用这些化合物。在某些实施方案中,治疗方法包括将本文提供的化合物与第二种制剂结合施用。还公开了包含本发明化合物的药物组合物和单一单位剂型。
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