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5-chloro-2-methoxy-β-[3,5-bis(trifluoromethyl)phenyl]styrene | 634187-22-7

中文名称
——
中文别名
——
英文名称
5-chloro-2-methoxy-β-[3,5-bis(trifluoromethyl)phenyl]styrene
英文别名
5-Chloro-2-methoxy-beta-[3,5-bis(trifluoromethyl)phenyl]styrene;1-[2-(5-chloro-2-methoxyphenyl)ethenyl]-3,5-bis(trifluoromethyl)benzene
5-chloro-2-methoxy-β-[3,5-bis(trifluoromethyl)phenyl]styrene化学式
CAS
634187-22-7
化学式
C17H11ClF6O
mdl
——
分子量
380.717
InChiKey
IUJFDTKHBYSIKX-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):
    6.6
  • 重原子数:
    25
  • 可旋转键数:
    3
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    9.2
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为产物:
    描述:
    3,5-二(三氟甲基)苯乙烯5-氯-2-甲氧基苯胺 在 tetrafluoroboric acid 、 sodium nitrite 作用下, 以 甲醇 为溶剂, 反应 2.0h, 以33.3%的产率得到5-chloro-2-methoxy-β-[3,5-bis(trifluoromethyl)phenyl]styrene
    参考文献:
    名称:
    EP1510207
    摘要:
    公开号:
点击查看最新优质反应信息

文献信息

  • Inhibitors against the activation of ap-1 and nfat
    申请人:Muto Susumu
    公开号:US20060100257A1
    公开(公告)日:2006-05-11
    A medicament inhibiting the activation of AP-1 which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to 5 (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种药物,抑制AP-1的激活,其活性成分为以下通式(I)所表示的化合物或其药学上可接受的盐、水合物或溶剂化物中所选的一种,其中X代表连接基,其主链中的原子数为2至5(该连接基可以被取代),A代表氢原子或乙酰基,E代表芳基或取代的杂芳基,环Z代表芳烃,除了由式—O-A所表示的基团外,可能还有一个或多个取代基,其中A具有上述定义的相同含义,由式—X-E所表示的基团中,X和E的每一个具有上述定义的相同含义,或者是一个杂芳烃,可能还有一个或多个取代基,其中A具有上述定义的相同含义,由式—X-E所表示的基团中,X和E的每一个具有上述定义的相同含义。
  • Medicament for treatment of diabetes
    申请人:Muto Susumu
    公开号:US20060111409A1
    公开(公告)日:2006-05-25
    A medicament for preventive and/or therapeutic treatment of diabetes or complications of diabetes which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to 5 (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O— A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种用于预防和/或治疗糖尿病或糖尿病并发症的药物,其活性成分为以下通式(I)所表示的化合物或其药学上可接受的盐、水合物或溶剂化物之一: 其中,X代表主链中原子数为2到5的连接基(该连接基可以被取代),A代表氢原子或乙酰基,E代表可以被取代的芳基或杂环芳基,环Z代表可以具有一个或多个取代基的芳基,除了由公式—O—A所表示的基团外,该芳基可以具有公式—X-E所表示的基团,其中每个X和E的含义与上述定义相同,或者可以具有一个或多个取代基的杂环芳基,除了由公式—O—A所表示的基团外,该杂环芳基可以具有公式—X-E所表示的基团,其中每个X和E的含义与上述定义相同。
  • Antiallergic
    申请人:Muto Susumu
    公开号:US20060122243A1
    公开(公告)日:2006-06-08
    A medicament for the preventive and/or therapeutic treatment of allergic diseases and/or endometriosis and/or hysteromyoma which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to 5 (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种用于预防和/或治疗过敏性疾病和/或子宫内膜异位症和/或子宫肌瘤的药物,其包括以下通式(I)所表示的化合物或其药学上可接受的盐、水合物和溶剂化物作为活性成分,其中X代表主链中原子数为2到5的连接基(该连接基可以被取代),A代表氢原子或乙酰基,E代表可以被取代的芳基或杂环芳基,环Z代表可以具有一个或多个取代基的芳烃,除了由公式-O-A所表示的基团外,该芳烃还可以具有公式—X-E所表示的基团,其中每个X和E具有上述定义的相同含义,或者该环可以具有一个或多个取代基,除了由公式—O-A所表示的基团外,该环还可以具有公式—X-E所表示的基团,其中A具有上述定义的相同含义,X和E分别具有上述定义的相同含义。
  • Immunity-related protein kinase inhibitors
    申请人:Muto Susumu
    公开号:US20060019958A1
    公开(公告)日:2006-01-26
    A medicament having an inhibitory activity against IKK-β and/or MEKK-1 or other protein kinases structurally similar thereto, which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to 5 (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substituents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种药物具有对IKK-β和/或MEKK-1或其他结构相似的蛋白激酶的抑制活性,其包括以下通式(I)所表示的化合物或其药学上可接受的盐,以及其水合物和溶剂化物作为活性成分的物质:其中,X表示连接主链中原子数为2至5的连接基(该连接基可以被取代),A表示氢原子或乙酰基,E表示可以被取代的芳基或取代的杂环芳基,环Z表示可以具有一个或多个取代基的芳烃,除了由式-O-A表示的基团外,该芳烃还可以具有式-X-E所表示的基团,其中每个X和E的含义与上述定义相同,或者是可以具有一个或多个取代基的杂环芳烃,除了由式-O-A表示的基团外,该杂环芳烃还可以具有式-X-E所表示的基团,其中每个X和E的含义与上述定义相同。
  • Antiallergic agents
    申请人:Muto Susumu
    公开号:US20070185059A1
    公开(公告)日:2007-08-09
    A medicament for the preventive and/or therapeutic treatment of allergic diseases and/or endometriosis and/or hysteromyoma which comprises as an active ingredient a substance selected from the group consisting of a compound represented by the following general formula (I) and a pharmacologically acceptable salt thereof, and a hydrate thereof and a solvate thereof: wherein X represents a connecting group whose number of atoms in the main chain is 2 to (said connecting group may be substituted), A represents hydrogen atom or acetyl group, E represents an aryl group which may be substituted or a hetero aryl group which may be substituted, ring Z represents an arene which may have one or more substitutents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above, or a heteroarene which may have one or more substitutents in addition to the group represented by formula —O-A wherein A has the same meaning as that defined above and the group represented by formula —X-E wherein each of X and E has the same meaning as that defined above.
    一种用于预防和/或治疗过敏性疾病和/或子宫内膜异位症和/或子宫肌瘤的药物,其活性成分包括以下通式(I)表示的化合物或其药学上可接受的盐、水合物和溶剂化物中的一种,其中X代表连接基,其主链中的原子数为2到(该连接基可以被取代),A代表氢原子或乙酰基,E代表芳基或取代的杂环芳基,环Z代表芳烃,除了由公式-O-A表示的基团外,还可以有一个或多个取代基,其中A具有上述定义的相同含义,并且由公式-X-E表示的基团,其中X和E的每个都具有上述定义的相同含义,或者可以有一个或多个取代基的杂芳烃,其中A具有上述定义的相同含义,并且由公式-X-E表示的基团,其中X和E的每个都具有上述定义的相同含义。
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