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1-(4-hydroxyphenyl)-2,2-dimethylpropan-1-one | 72569-10-9

中文名称
——
中文别名
——
英文名称
1-(4-hydroxyphenyl)-2,2-dimethylpropan-1-one
英文别名
——
1-(4-hydroxyphenyl)-2,2-dimethylpropan-1-one化学式
CAS
72569-10-9
化学式
C11H14O2
mdl
——
分子量
178.231
InChiKey
GTFQCBPFABJXEM-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:
    90 °C
  • 沸点:
    309.8±15.0 °C(Predicted)
  • 密度:
    1.054±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.6
  • 重原子数:
    13
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.36
  • 拓扑面积:
    37.3
  • 氢给体数:
    1
  • 氢受体数:
    2

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

点击查看最新优质反应信息

文献信息

  • [EN] HCV POLYMERASE INHIBITORS<br/>[FR] INHIBITEURS DE LA POLYMÉRASE DU VHC
    申请人:MEDIVIR AB
    公开号:WO2015056213A1
    公开(公告)日:2015-04-23
    The invention provides compounds of the formula (I) wherein B is a nucleobase selected from the groups (a) to (d): and the other variables are as defined in the claims, which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.
    这项发明提供了公式(I)中的化合物,其中B是从(a)到(d)组中选择的核碱基:其他变量如索权中所定义,这些化合物可用于治疗或预防丙型肝炎病毒感染及相关方面。
  • [EN] DIOXOLANE ANALOGUES OF URIDINE FOR THE TREATMENT OF CANCER<br/>[FR] ANALOGUES DIOXOLANE D'URIDINE POUR LE TRAITEMENT DU CANCER
    申请人:MEDIVIR AB
    公开号:WO2016030335A1
    公开(公告)日:2016-03-03
    The invention provides compounds of formula (I), wherein: R1 is OR11, or NR5R5'; R2 is H or F; R5 is H, C1-C6alkyl, OH, C(=O)R6, O(C=O)R6 or O(C=O)OR6; R5´ is H or C1-C6alkyl; R6 is C1-C6alkyl or C3-C7cycloalkyl; R13 is H, phenyl, pyridyl, benzyl, indolyl or naphthyl wherein the phenyl, pyridyl, benzyl, indolyl and naphthyl is optionally substituted with 1, 2 or 3 R22; and the other variables are as defined in the claims, which are of use in the treatment of cancer, and related aspects.
    这项发明提供了式(I)的化合物,其中:R1为OR11或NR5R5';R2为H或F;R5为H、C1-C6烷基、OH、C(=O)R6、O(C=O)R6或O(C=O)OR6;R5´为H或C1-C6烷基;R6为C1-C6烷基或C3-C7环烷基;R13为H、苯基、吡啶基、苄基、吲哚基或基,其中苯基、吡啶基、苄基、吲哚基和基可选择地被1、2或3个R22取代;其他变量如索权中所定义,用于癌症治疗及相关方面。
  • ACYLBENZENE DERIVATIVE
    申请人:Yamanoi Shigeo
    公开号:US20130217733A1
    公开(公告)日:2013-08-22
    Provided are compounds having an excellent hypoglycemic action and a β cell- or pancreas-protecting action or a pharmaceutically acceptable salt thereof, and a pharmaceutical composition having an excellent therapeutic effect and/or prophylactic effect on type 1 diabetes, type 2 diabetes, and the like, which cause an increase in the blood sugar level due to abnormal sugar metabolism. A compound represented by general formula (I), or a pharmaceutically acceptable salt thereof, is disclosed.
    提供了具有优异降糖作用和β细胞或胰腺保护作用或其药用盐的化合物,以及具有优异治疗效果和/或预防Ⅰ型糖尿病、Ⅱ型糖尿病等引起血糖平升高的药物组合物。公开了一种由通用式(I)表示的化合物或其药用盐。
  • [EN] FUNGICIDAL COMPOSITION CONTAINING ACID AMIDE DERIVATIVE<br/>[FR] COMPOSITION FONGICIDE CONTENANT UN DÉRIVÉ D'AMIDE D'ACIDE
    申请人:ISHIHARA SANGYO KAISHA
    公开号:WO2006016708A1
    公开(公告)日:2006-02-16
    Conventional many fungicidal compositions have had practical problems such that either a preventive effect or a curing effect is inadequate, the residual effect tends to be inadequate, or the controlling effect against plant diseases tends to be inadequate depending upon the application site, and a fungicidal composition to overcome such problems has been desired. The present invention provides a fungicidal composition containing an acid amide derivative of the formula (I) or a salt thereof, as an active ingredient: wherein A is phenyl which may be substituted, benzyl which may be substituted, naphthyl which may be substituted, heterocyclic ring which may be substituted, fused heterocyclic ring which may be substituted, or the like; B is heterocyclic ring which may be substituted, fused heterocyclic ring which may be substituted, or naphthyl which may be substituted; each of R1 and R2 which are independent of each other, is alkyl, or the like; R3 is hydrogen, or the like; each of W1 and W2 which are independent of each other, is oxygen or sulfur.
    传统的许多杀真菌组合物存在实际问题,例如预防效果或治疗效果不足,残留效果往往不足,或者根据应用场所,控制植物病害的效果往往不足,因此需要一种能够克服这些问题的杀真菌组合物。本发明提供了一种含有式(I)的酸酰胺衍生物或其盐的杀真菌组合物作为活性成分:其中A是苯基,可能被取代,苄基,可能被取代,基,可能被取代,杂环环,可能被取代,融合的杂环环,可能被取代,或类似物;B是可能被取代的杂环环,融合的可能被取代的杂环环,或可能被取代的基;R1和R2各自独立的,是烷基,或类似物;R3是氢,或类似物;W1和W2各自独立的,是氧或
  • HCV POLYMERASE INHIBITORS
    申请人:MEDIVIR AB
    公开号:US20150175648A1
    公开(公告)日:2015-06-25
    The invention provides compounds of the formula: wherein B is a nucleobase selected from the groups (a) to (d): and the other variables are as defined in the claims, which are of use in the treatment or prophylaxis of hepatitis C virus infection, and related aspects.
    该发明提供了以下式子的化合物:其中B是从(a)到(d)组中选择的核苷碱:其他变量如权利要求中所定义,这些化合物可用于治疗或预防丙型肝炎病毒感染及相关方面。
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