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[4-(2-甲基-3-丁烯-2-基)-1H-咪唑-5-基]甲醇 | 316148-59-1

中文名称
[4-(2-甲基-3-丁烯-2-基)-1H-咪唑-5-基]甲醇
中文别名
1H-吡唑-3-羧酸,5-甲基-,1-甲基酰肼
英文名称
(5-(1,1-dimethyl-2-propenyl)imidazole-4-yl)methanol
英文别名
[5-(1,1-dimethyl-allyl)-3H-imidazol-4-yl]-methanol;[4-(2-methylbut-3-en-2-yl)-1H-imidazol-5-yl]methanol
[4-(2-甲基-3-丁烯-2-基)-1H-咪唑-5-基]甲醇化学式
CAS
316148-59-1
化学式
C9H14N2O
mdl
——
分子量
166.223
InChiKey
DOSITEMRMPTXEY-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:
    171-173 °C
  • 沸点:
    344.9±32.0 °C(Predicted)
  • 密度:
    1.085±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    1.2
  • 重原子数:
    12
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.44
  • 拓扑面积:
    48.9
  • 氢给体数:
    2
  • 氢受体数:
    2

SDS

SDS:81fdfcb65ffabdda410efb62b42b6901
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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

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文献信息

  • ANALOGS OF DEHYDROPHENYLAHISTINS AND THEIR THEAPEUTIC USE
    申请人:Palladino Michael A.
    公开号:US20080221122A1
    公开(公告)日:2008-09-11
    Compounds represented by the following structure (II) are disclosed: as are methods for making such compounds. Compositions and methods for treating various disease conditions including cancer and non-cancer diseases associated with vascular proliferation are also disclosed.
    由以下结构(II)表示的化合物已被披露:制备这种化合物的方法也已被披露。还披露了用于治疗各种疾病条件的组合物和方法,包括与血管增殖相关的癌症和非癌症疾病。
  • Dehydrophenylahistins and analogs thereof and the synthesis of dehydrophenylahistins and analogs thereof
    申请人:Palladino A. Michael
    公开号:US20050197344A1
    公开(公告)日:2005-09-08
    Compounds represented by the following structure (I) are disclosed: as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R 1 , R 1 ′, R 1 ″, R 2 , R 3 , R 4 , R 5 , and R 6 , X 1 and X 2 , Y, Z, Z 1 , Z 2 , Z 3 , and Z 4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating vascular proliferation are also disclosed.
    公开了以下结构(I)代表的化合物:制备这种化合物的方法也被公开,其中所述方法包括将二酰基二酮哌嗪与第一醛反应以产生中间化合物;然后将中间化合物与第二醛反应,以产生具有通用结构的化合物类,其中第一醛和第二醛选自氧唑羧醛,咪唑羧醛,苯甲醛,咪唑羧醛衍生物和苯甲醛衍生物组成的群体,从而形成上述化合物,其中R1、R1'、R1''、R2、R3、R4、R5和R6,X1和X2,Y,Z,Z1,Z2,Z3和Z4可以分别根据附带说明书中的描述进行定义。还公开了用于治疗血管增殖的组合物和方法。
  • [EN] DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF AND THE SYNTHESIS OF DEHYDROPHENYLAHISTINS AND ANALOGS THEREOF<br/>[FR] DESHYDROPHENYLAHISTINES ET ANALOGUES DE CEUX-CI ET SYNTHESE DE CES DESHYDROPHENYLAHISTINES ET D'ANALOGUES DE CEUX-CI
    申请人:NEREUS PHARMACEUTICALS INC
    公开号:WO2004054498A2
    公开(公告)日:2004-07-01
    Compounds represented by structure (I) are disclosed, as are methods for making such compounds, wherein said methods comprise reacting a diacyldiketopiperazine with a first aldehyde to produce an intermediate compound; and reacting the intermediate compound with a second aldehyde to produce the class of compounds with the generic structure, where the first aldehyde and the second aldehydes are selected from the group consisting of an oxazolecarboxaldeyhyde, imidazolecarboxaldehyde, a benzaldehyde, imidazolecarboxaldehyde derivatives, and benzaldehyde derivatives, thereby forming the above compound wherein R1, R1', R1'', R2, R3, R4, R5, and R6, X1 and X2, Y, Z, Z1, Z2, Z3, and Z4 may each be separately defined in a manner consistent with the accompanying description. Compositions and methods for treating cancer and fungal infection are also disclosed.
    本发明揭示了结构(I)所代表的化合物,以及制备此类化合物的方法,其中所述方法包括将双酰基二酮哌嗪与第一醛反应以产生中间化合物;并将中间化合物与第二醛反应以产生具有通用结构的化合物类别,其中第一醛和第二醛选自羧醛噁唑,咪唑羧醛,苯甲醛,咪唑羧醛衍生物和苯甲醛衍生物的群体,从而形成上述化合物,其中R1,R1',R1'',R2,R3,R4,R5和R6,X1和X2,Y,Z,Z1,Z2,Z3和Z4可以分别按照所附说明书的方式定义。本发明还揭示了用于治疗癌症和真菌感染的组合物和方法。
  • Analogs of dehydrophenylahistins and their therapeutic use
    申请人:Palladino Michael
    公开号:US20070078138A1
    公开(公告)日:2007-04-05
    Compounds represented by the following structure (II) are disclosed: as are methods for making such compounds. Compositions and methods for treating various disease conditions including cancer and non-cancer diseases associated with vascular proliferation are also disclosed.
    本文揭示了由以下结构(II)所代表的化合物,以及制造这种化合物的方法。此外,还揭示了用于治疗各种疾病状况的组合物和方法,包括与血管增殖有关的癌症和非癌症疾病。
  • ANALOGS OF DEHYDROPHENYLAHISTINS AND THEIR THERAPEUTIC USE
    申请人:Palladino Michael
    公开号:US20120277251A1
    公开(公告)日:2012-11-01
    Compounds represented by the following structure (II) are disclosed: as are methods for making such compounds. Compositions and methods for treating various disease conditions including cancer and non-cancer diseases associated with vascular proliferation are also disclosed.
    本文披露了以下结构(II)所代表的化合物,以及制备这些化合物的方法。此外,还披露了用于治疗各种疾病状况的组合物和方法,包括与血管增生相关的癌症和非癌性疾病。
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