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4-乙氧基苯甲酰基乙腈 | 54605-62-8

中文名称
4-乙氧基苯甲酰基乙腈
中文别名
对甲氧基-X-腈基-苯乙酮;3-(4-乙氧苯基)-3-氧代丙腈;3-(4-乙氧基苯基)-3-氧代丙腈;3-(4-甲氧苯基)-3-氧代丙腈
英文名称
4-ethoxyphenyl-3-oxopropanenitrile
英文别名
p-Aethoxybenzoylacetonitril;ω-cyano-4-ethoxyacetophenone;p-ethoxy-benzoylacetonitrile;3-(4-ethoxy-phenyl)-3-oxo-propionitrile;3-Oxo-3-(4-aethoxy-phenyl)-propionsaeure-nitril;3-(4-Aethoxy-phenyl)-3-oxo-propionitril;4-Aethoxy-benzoylessigsaeurenitril;4-Aethoxy-benzoylacetonitril;4-Cyanacetyl-phenetol;3-(4-ethoxyphenyl)-3-oxopropanenitrile
4-乙氧基苯甲酰基乙腈化学式
CAS
54605-62-8
化学式
C11H11NO2
mdl
MFCD02260795
分子量
189.214
InChiKey
CJZHUVVJWMKTPH-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

  • 熔点:
    128-130°

计算性质

  • 辛醇/水分配系数(LogP):
    1.3
  • 重原子数:
    14
  • 可旋转键数:
    4
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.27
  • 拓扑面积:
    50.1
  • 氢给体数:
    0
  • 氢受体数:
    3

安全信息

  • 危险等级:
    IRRITANT
  • 海关编码:
    2926909090

SDS

SDS:01197b666b5cab38a7365df1d39325d5
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反应信息

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文献信息

  • Pyrazolo-pyrrolo-pyrimidine-diones
    申请人:The Upjohn Company
    公开号:US05132424A1
    公开(公告)日:1992-07-21
    New pyrazolo-pyrrolo-pyrimidine-dione (PPPD) compounds of formula (I), ##STR1## where R.sub.1, R.sub.2, R.sub.3, R.sub.4 and m are as defined in the specification, e.g., 4-(benzoylmethyl)-6-cyclohexyl-6,7-dihydro-2-phenyl-4H-pyrazolo[1,5-a]pyrr olo[3,4-d]pyrimidine-5,8-dione, have been found to be potentially useful to treat warm-blooded animal patients suffering from the symptoms of atherosclerosis and cholesterol buildup to relieve the same and for favorably altering the high density lipoprotein (HDL) to low density lipoprotein (LDL) ratio in blood samples of such patients.
    新型吡唑并吡咯并嘧啶二酮(PPPD)化合物,其化学式为(I),##STR1## 其中R₁、R₂、R₃、R₄和m的定义如说明书所述,例如,4-(苯甲酰甲基)-6-环己基-6,7-二氢-2-苯基-4H-吡唑[1,5-a]吡咯[3,4-d]嘧啶-5,8-二酮,被发现对治疗热血动物患者动脉粥样硬化和胆固醇积聚的症状具有潜在的有用性,以缓解这些症状,并有利于改变这些患者血液样本中高密度脂蛋白(HDL)与低密度脂蛋白(LDL)的比例。
  • Synthesis and hypocholesterolemic activity of 6,7-dihydro-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-diones, novel inhibitors of acylCoA: cholesterol O-acyltransferase
    作者:Scott D. Larsen、Charles H. Spilman、Frank P. Bell、Dac M. Dinh、Esther Martinborough、Gracella J. Wilson
    DOI:10.1021/jm00109a028
    日期:1991.5
    A novel series of 6,7-dihydro-4H-pyrazolo[1,5-a]pyrrolo[3,4-d]pyrimidine-5,8-dione inhibitors of the enzyme acyl-CoA:cholesterol O-acyltransferase is described. A number of these derivatives were found to be potent modulators of serum lipoprotein levels in cholesterol-fed rats. Further evaluation of one of the most effective analogues confirmed that it was significantly blocking the absorption of cholesterol
    描述了酶-CoA:胆固醇O-酰基转移酶的一系列新的6,7-二氢-4H-吡唑并[1,5-a]吡咯并[3,4-d]嘧啶-5,8-二酮抑制剂。发现这些衍生物中的许多是胆固醇喂养的大鼠中血清脂蛋白水平的有效调节剂。对最有效的类似物之一的进一步评估证实,它明显阻止了肠道中胆固醇的吸收。
  • 3-(heteroarylamino)methylene-1,3-dihydro-2H-indol-2-ones as kinase inhibitors
    申请人:Allergan, Inc.
    公开号:US06559173B1
    公开(公告)日:2003-05-06
    The present invention relates to organic molecules capable of modulating tyrosine kinase signal transduction in order to regulate, modulate and/or inhibit abnormal cell proliferation.
    本发明涉及有机分子,能够调节酪氨酸激酶信号传导,以调控、调节和/或抑制异常细胞增殖。
  • [EN] TRI- AND TETRACYCLIC PYRAZOLO[3,4-B]PYRIDINE COMPOUNDS AS ANTINEOPLASTIC AGENT<br/>[FR] COMPOSÉS TRICYCLIQUES ET TÉTRACYCLIQUES DE PYRAZOLO[3,4-B]PYRIDINE EN TANT QU'AGENT ANTINÉOPLASIQUE
    申请人:PF MEDICAMENT
    公开号:WO2012140114A1
    公开(公告)日:2012-10-18
    The present invention relates to compounds of following general formula (I): and to the pharmaceutically acceptable salts of same, the tautomers of same, the stereoisomers or mixture of stereoisomers in any proportions of same, such as a mixture of enantiomers, notably a racemic mixture, as well as to methods for preparing same and uses of same, notably as an antineoplastic agent.
    本发明涉及以下一般式(I)的化合物,以及同一化合物的药用可接受盐,同分异构体,立体异构体或同分异构体的混合物,例如对映体混合物,尤其是消旋混合物,以及制备同一化合物的方法和用途,尤其是作为抗肿瘤剂。
  • TRI - AND TETRACYCLIC PYRAZOLO[3,4-B]PYRIDINE COMPOUNDS AS ANTINEOPLASTIC AGENT
    申请人:Rabot Rémi
    公开号:US20140031362A1
    公开(公告)日:2014-01-30
    The present invention relates to compounds of following general formula (I): and to the pharmaceutically acceptable salts of same, the tautomers of same, the stereoisomers or mixture of stereoisomers in any proportions of same, such as a mixture of enantiomers, notably a racemic mixture, as well as to methods for preparing same and uses of same, notably as an antineoplastic agent.
    本发明涉及以下一般式(I)的化合物,以及其药学上可接受的盐,同分异构体,立体异构体或其混合物,如对映体混合物,特别是消旋混合物,以及制备同样的方法和用途,特别是作为抗肿瘤药物。
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