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1-(3,3,3-trifluoropropylthio)-4-bromobenzene | 403793-25-9

中文名称
——
中文别名
——
英文名称
1-(3,3,3-trifluoropropylthio)-4-bromobenzene
英文别名
1-bromo-4-(3,3,3-trifluoropropylsulfanyl)benzene
1-(3,3,3-trifluoropropylthio)-4-bromobenzene化学式
CAS
403793-25-9
化学式
C9H8BrF3S
mdl
——
分子量
285.128
InChiKey
UELKIIFZVNFDDY-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):
    4.6
  • 重原子数:
    14
  • 可旋转键数:
    3
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.33
  • 拓扑面积:
    25.3
  • 氢给体数:
    0
  • 氢受体数:
    4

上下游信息

  • 下游产品
    中文名称 英文名称 CAS号 化学式 分子量

反应信息

  • 作为反应物:
    描述:
    1-(3,3,3-trifluoropropylthio)-4-bromobenzeneOxone 作用下, 以 甲醇 为溶剂, 反应 18.0h, 以95%的产率得到1-(3,3,3-Trifluoropropylsulphonyl)-4-bromobenzene
    参考文献:
    名称:
    Imidazolo-5-YL-2anilino-pyrimidines as agents for the inhibition of the cell proliffration
    摘要:
    该公式化合物(I):其中R1、R2、R3、R4、R5、R6、p、q和n的定义如下,并描述了其药用盐和体内可水解酯。还描述了它们的制备过程以及它们作为药物的用途,特别是作为用于在温血动物(如人)中产生细胞周期抑制(抗细胞增殖)作用的药物。
    公开号:
    US20040014776A1
  • 作为产物:
    描述:
    3-溴-1,1,1-三氟丙烷4-溴苯硫酚potassium carbonate 作用下, 以 DMF (N,N-dimethyl-formamide) 为溶剂, 反应 1.0h, 以95%的产率得到1-(3,3,3-trifluoropropylthio)-4-bromobenzene
    参考文献:
    名称:
    Imidazolo-5-YL-2anilino-pyrimidines as agents for the inhibition of the cell proliffration
    摘要:
    该公式化合物(I):其中R1、R2、R3、R4、R5、R6、p、q和n的定义如下,并描述了其药用盐和体内可水解酯。还描述了它们的制备过程以及它们作为药物的用途,特别是作为用于在温血动物(如人)中产生细胞周期抑制(抗细胞增殖)作用的药物。
    公开号:
    US20040014776A1
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文献信息

  • [EN] DERIVATIVES OF 4- (IMIDAZOL-5-YL)-2-(4-SULFOANILINO) PYRIMIDINE WITH CDK INHIBITORY ACTIVITY<br/>[FR] DERIVES DE 4- (IMIDAZOL-5-YL)-2-(4-SULFOANILINO) PYRIMIDINE A ACTIVITE INHIBITRICE CDK
    申请人:ASTRAZENECA AB
    公开号:WO2003076436A1
    公开(公告)日:2003-09-18
    Compounds of the formula (I): wherein R1, R2, R3, R4, R5 and p are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.
    公式(I)的化合物:其中R1、R2、R3、R4、R5和p的定义如下,并且描述了药学上可接受的盐和体内可解酯。还描述了它们的制备过程以及它们作为药物的用途,特别是作为用于在温血动物(如人)中产生细胞周期抑制(抗细胞增殖)效果的药物。
  • Derivatives of 4-(imidazol-5-yl)-2-(4-sulfoanilino)pyrimidine with cdk inhibitory activity
    申请人:Newcombe John Nicholas
    公开号:US20050131000A1
    公开(公告)日:2005-06-16
    Compounds of the formula (I): wherein R 1 , R 2 , R 3 , R 4 , R 5 and p are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.
    本文描述了化学式(I)的化合物,其中R1、R2、R3、R4、R5和p的定义如本文中所述,并描述了其药物学上可接受的盐和体内可解的酯。同时还描述了它们的制备过程以及它们作为药物的用途,特别是作为产生对温血动物(如人)的细胞周期抑制(抗细胞增殖)效应的药物。
  • Imidazolo-5-yl-2-anilino-pyrimidines as agents for the inhibition of the cell proliferation
    申请人:Breault Anne Gloria
    公开号:US20060004033A1
    公开(公告)日:2006-01-05
    Compounds of the formula (I): wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , p, q, and n are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.
    式(I)的化合物:其中R1、R2、R3、R4、R5、R6、p、q和n的定义如内部所述,并且所述化合物的药学上可接受的盐和体内可解的酯被描述。还描述了它们的制备过程以及它们作为药物的用途,特别是作为在温血动物(如人)中产生细胞周期抑制(抗细胞增殖)效应的药物。
  • Derivatives of 4-(imidazol-5-yl)-2-(4-sulfoanilino)pyrimidine with CDK inhibitory activity
    申请人:AstraZeneca AB
    公开号:US07465728B2
    公开(公告)日:2008-12-16
    Compounds of the formula (I): wherein R1, R2, R3, R4, R5 and p are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.
    本发明涉及式(I)的化合物,其中R1、R2、R3、R4、R5和p如定义所述,并描述了其药学上可接受的盐和体内可解的酯。还描述了它们的制备过程以及它们作为药物的用途,特别是作为在温血动物(例如人)中产生细胞周期抑制(抗细胞增殖)效应的药物。
  • Imidazolo-5-YL-2-anilino-pyrimidines as agents for the inhibition of the cell proliferation
    申请人:Breault Gloria Anne
    公开号:US06969714B2
    公开(公告)日:2005-11-29
    Compounds of the formula (I): wherein R 1 , R 2 , R 3 , R 4 , R 5 , R 6 , p, q, and n are as defined within and a pharmaceutically acceptable salts and in vivo hydrolysable esters are described. Also described are processes for their preparation and their use as medicaments, particularly medicaments for producing a cell cycle inhibitory (anti-cell-proliferation) effect in a warm-blooded animal, such as man.
    该式(I)的化合物:其中R1、R2、R3、R4、R5、R6、p、q和n的定义如内部所述,并描述了其药学上可接受的盐和体内可解的酯。还描述了它们的制备过程以及它们作为药物的用途,特别是作为制造细胞周期抑制(抗细胞增殖)效应的药物,用于温血动物,例如人类。
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