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trifluoromethanesulfonic acid 2,6-dimethylpyridin-4-yl ester | 129558-60-7

中文名称
——
中文别名
——
英文名称
trifluoromethanesulfonic acid 2,6-dimethylpyridin-4-yl ester
英文别名
2,6-dimethyl-pyridin-4-yl trifluoromethanesulfonate;(2,6-dimethylpyridin-4-yl) trifluoromethanesulfonate
trifluoromethanesulfonic acid 2,6-dimethylpyridin-4-yl ester化学式
CAS
129558-60-7
化学式
C8H8F3NO3S
mdl
——
分子量
255.218
InChiKey
DKLSQHIVJRCFMG-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

  • 沸点:
    281.8±40.0 °C(Predicted)
  • 密度:
    1.444±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.4
  • 重原子数:
    16
  • 可旋转键数:
    2
  • 环数:
    1.0
  • sp3杂化的碳原子比例:
    0.38
  • 拓扑面积:
    64.6
  • 氢给体数:
    0
  • 氢受体数:
    7

反应信息

  • 作为反应物:
    描述:
    trifluoromethanesulfonic acid 2,6-dimethylpyridin-4-yl ester1-(4-硝基苯基)哌嗪 、 Brine 、 Sodium sulfate-III 、 crude material 、 silica gel 作用下, 以 二乙二醇二甲醚氯仿 为溶剂, 反应 0.67h, 以to afford 4-[4-(2,6-dimethyl-pyridin-4-yl)-1-(4-nitrophenyl)-piperazine (0.30 g, 49%) as a yellow solid的产率得到4-(4-(2,6-dimethylpyridin-4-yl))-1-(4-nitrophenyl)piperazine
    参考文献:
    名称:
    2- [ (2-SUBSTITUTED) -IND0LIZIN-3-YL] -2-OXO-ACETAMIDE DERIVATIVES AS ANTIFUNGAL AGENTS
    摘要:
    该发明提供了公式(I)的化合物及其药学上可接受的盐,其中:R1,R2,R3,R4,R5,R6,R7,X和X1如本文所定义。这些化合物在制造用于预防或治疗真菌病的药物方面是有用的。公式(I)的化合物及其农业上可接受的盐也可用作农业杀真菌剂。
    公开号:
    US20100056511A1
  • 作为产物:
    描述:
    脱氢乙酸三乙胺 作用下, 以 二氯甲烷 为溶剂, 反应 2.41h, 生成 trifluoromethanesulfonic acid 2,6-dimethylpyridin-4-yl ester
    参考文献:
    名称:
    WO2008/57469
    摘要:
    公开号:
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文献信息

  • Small organic molecule regulators of cell proliferation
    申请人:Brunton Shirley Ann
    公开号:US20080182859A1
    公开(公告)日:2008-07-31
    The present invention makes available methods and reagents for modulating proliferation or differentiation in a cell or tissue comprising contacting the cell with a compound. In certain embodiments, the methods and reagents may be employed to correct or inhibit an aberrant or unwanted growth state, e.g., by antagonizing a normal patched pathway or agonizing smoothened or hedgehog activity.
    本发明提供了一种调节细胞或组织增殖或分化的方法和试剂,包括将细胞与化合物接触。在某些实施例中,该方法和试剂可用于纠正或抑制异常或不需要的生长状态,例如通过拮抗正常的Patched途径或激活Smoothened或Hedgehog活性。
  • Processes for the preparation of compounds
    申请人:Krishnan Lalitha
    公开号:US20080058521A1
    公开(公告)日:2008-03-06
    The present invention provides improved synthetic methods for the preparation of compounds that modulate proliferation or differentiation in a cell or tissue.
    本发明提供了改进的合成方法,用于制备能够调节细胞或组织增殖或分化的化合物。
  • SMALL ORGANIC MOLECULE REGULATORS OF CELL PROLIFERATION
    申请人:Brunton Shirley Ann
    公开号:US20120245184A1
    公开(公告)日:2012-09-27
    The present invention makes available methods and reagents for modulating proliferation or differentiation in a cell or tissue comprising contacting the cell with a compound. In certain embodiments, the methods and reagents may be employed to correct or inhibit an aberrant or unwanted growth state, e.g., by antagonizing a normal patched pathway or agonizing smoothened or hedgehog activity.
    本发明提供了一种调节细胞或组织增殖或分化的方法和试剂,包括将细胞与化合物接触。在某些实施例中,这些方法和试剂可用于纠正或抑制异常或不良的生长状态,例如通过拮抗正常的Patched通路或激活Smoothened或Hedgehog活性。
  • ANTIFUNGAL COMBINATION THERAPY
    申请人:Birch Michael
    公开号:US20110183969A1
    公开(公告)日:2011-07-28
    The invention provides pharmaceutical combinations comprising a combination of an antifungal indolizine compound of formula (I) or a pharmaceutically acceptable salt thereof and a second antifungal agent: wherein: R1, R2, R3, R4, R5, R6, R7, X and X 1 are as defined herein. The invention also provides pharmaceutical compositions comprising an antifungal indolizine compound of formula (I) or a pharmaceutically acceptable salt thereof, a second antifungal agent and a pharmaceutically acceptable diluent or carrier. The combinations and compositions are useful in the prevention or treatment of a fungal disease. A combination of an indolizine compound of formula (I) or agriculturally acceptable salts thereof and a second antifungal agent may also be used as an agricultural fungicide.
    本发明提供了药物组合物,包括式(I)的抗真菌吲哚啉化合物或其药学上可接受的盐和第二种抗真菌剂的组合:其中:R1,R2,R3,R4,R5,R6,R7,X和X1如本文所定义。本发明还提供了药物组合物,包括式(I)的抗真菌吲哚啉化合物或其药学上可接受的盐、第二种抗真菌剂和药学上可接受的稀释剂或载体。该组合物和组合物在预防或治疗真菌病方面是有用的。式(I)的吲哚啉化合物或其农业上可接受的盐和第二种抗真菌剂的组合也可用作农业杀菌剂。
  • 2-[(2-substituted)-indolizin-3-yl]-2-oxo-acetamide derivatives as antifungal agents
    申请人:Downham Robert
    公开号:US08604029B2
    公开(公告)日:2013-12-10
    The invention provides compounds of formula (I), and pharmaceutically acceptable salts thereof wherein: R1, R2, R3, R4, R5, R6, R7, X and X1 are as defined herein. These compounds are useful in the manufacture of medicaments for use in the prevention or treatment of a fungal disease. Compounds of formula (I), and agriculturally acceptable salts thereof, may also be used as agricultural fungicides.
    本发明提供了以下式子(I)的化合物及其药学上可接受的盐,其中:R1、R2、R3、R4、R5、R6、R7、X和X1的定义如本文所述。这些化合物可用于制造用于预防或治疗真菌病的药物。式(I)的化合物及其农业上可接受的盐也可用作农业杀菌剂。
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