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2-甲基-4,5,7-三氯喹啉 | 203626-80-6

中文名称
2-甲基-4,5,7-三氯喹啉
中文别名
——
英文名称
2-methyl-4,5,7-trichloroquinoline
英文别名
4,5,7-trichloro-2-methylquinoline
2-甲基-4,5,7-三氯喹啉化学式
CAS
203626-80-6
化学式
C10H6Cl3N
mdl
——
分子量
246.523
InChiKey
DSRVLGATYHLALY-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:
    333.9±37.0 °C(Predicted)
  • 密度:
    1.459±0.06 g/cm3(Predicted)
  • 溶解度:
    可溶于氯仿(少许)、甲醇(少许)

计算性质

  • 辛醇/水分配系数(LogP):
    4.5
  • 重原子数:
    14
  • 可旋转键数:
    0
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.1
  • 拓扑面积:
    12.9
  • 氢给体数:
    0
  • 氢受体数:
    1

安全信息

  • 危险品标志:
    T
  • 安全说明:
    S26,S39,S45
  • 危险类别码:
    R25,R41
  • WGK Germany:
    3

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:
    2-甲基-4,5,7-三氯喹啉一水合肼 作用下, 以 乙醇 为溶剂, 以80%的产率得到(5,7-Dichloro-2-methyl-quinolin-4-yl)-hydrazine
    参考文献:
    名称:
    Synthesis and anti-tubercular evaluation of 4-quinolylhydrazones
    摘要:
    A series of 4-quinolylhydrazones were synthesized and tested against Mycobacterium tuberculosis H37Rv. Preparation of the title compounds was achieved by reaction of 4-quinolylhydrazine and aryl- or heteroaryl-carboxaldehyde. For the most of derivatives interesting antitubercular properties were showed: two compounds (3(2) and 3(25)), identified as the most active, were tested also against Mycobacterium avium. (C) 2002 Elsevier Science Ltd. All rights reserved.
    DOI:
    10.1016/s0968-0896(02)00071-8
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文献信息

  • Synthesis and anti-tubercular evaluation of 4-quinolylhydrazones
    作者:Luisa Savini、Luisa Chiasserini、Alessandra Gaeta、Cesare Pellerano
    DOI:10.1016/s0968-0896(02)00071-8
    日期:2002.7
    A series of 4-quinolylhydrazones were synthesized and tested against Mycobacterium tuberculosis H37Rv. Preparation of the title compounds was achieved by reaction of 4-quinolylhydrazine and aryl- or heteroaryl-carboxaldehyde. For the most of derivatives interesting antitubercular properties were showed: two compounds (3(2) and 3(25)), identified as the most active, were tested also against Mycobacterium avium. (C) 2002 Elsevier Science Ltd. All rights reserved.
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