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4-(2,3,4-trifluoro-phenyl)-thiazol-2-ylamine | 881401-98-5

中文名称
——
中文别名
——
英文名称
4-(2,3,4-trifluoro-phenyl)-thiazol-2-ylamine
英文别名
4-(2,3,4-trifluorophenyl)-1,3-thiazol-2-amine
4-(2,3,4-trifluoro-phenyl)-thiazol-2-ylamine化学式
CAS
881401-98-5
化学式
C9H5F3N2S
mdl
——
分子量
230.213
InChiKey
GWQIWAKNKDCLPC-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):
    2.6
  • 重原子数:
    15
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    67.2
  • 氢给体数:
    1
  • 氢受体数:
    6

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

反应信息

点击查看最新优质反应信息

文献信息

  • FUROPYRIMIDINEDIONE DERIVATIVES AS TRPAI MODULATORS
    申请人:Chaudhari Sachin Sundarlal
    公开号:US20120178766A1
    公开(公告)日:2012-07-12
    The present invention is related to novel furopyrimidinedione derivatives as TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPA1 (Transient Receptor Potential subfamily A, member 1). Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPA1.
    本发明涉及新型噻吩嘧啶二酮衍生物作为TRPA(瞬时受体电位亚家族A)调节剂。特别地,本文所描述的化合物可用于治疗或预防由TRPA1(瞬时受体电位亚家族A,成员1)调节的疾病、情况和/或疾患。本文还提供了用于制备所述化合物的过程,用于其合成的中间体,其制药组合物以及用于治疗或预防由TRPA1调节的疾病、情况和/或疾患的方法。
  • TROMBOPOIETIN RECEPTOR AGONISTS
    申请人:Pfizer Products Incorporated
    公开号:EP1794156A2
    公开(公告)日:2007-06-13
  • FUROPYRIMIDINEDIONE DERIVATIVES AS TRPA1 MODULATORS
    申请人:Glenmark Pharmaceuticals S.A.
    公开号:EP2411395A1
    公开(公告)日:2012-02-01
  • [EN] TROMBOPOIETIN RECEPTOR AGONISTS<br/>[FR] AGONISTES DU RECEPTEUR DE THROMBOPOIETINE
    申请人:PFIZER PROD INC
    公开号:WO2006033005A2
    公开(公告)日:2006-03-30
    A compound of the formula (I) useful as promoters of thrombopoiesis and megakaryocytopoiesis, wherein A, B, D, E, W, X, Y, Z, R1 and R2 are defined as above.
  • [EN] FUROPYRIMIDINEDIONE DERIVATIVES AS TRPA1 MODULATORS<br/>[FR] DÉRIVÉS DE FUROPYRIMIDINEDIONE À TITRE DE MODULATEURS DE TRPA1
    申请人:GLENMARK PHARMACEUTICALS SA
    公开号:WO2010109329A1
    公开(公告)日:2010-09-30
    The present invention is related to novel furopyrimidinedione derivatives as TRPA (Transient Receptor Potential subfamily A) modulators. In particular, compounds described herein are useful for treating or preventing diseases, conditions and/or disorders modulated by TRPAl (Transient Receptor Potential subfamily A, member 1). Also provided herein are processes for preparing compounds described herein, intermediates used in their synthesis, pharmaceutical compositions thereof, and methods for treating or preventing diseases, conditions and/or disorders modulated by TRPAl. (Formula I) (I)
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