摩熵化学
数据库官网
小程序
打开微信扫一扫
首页 分子通 化学资讯 化学百科 反应查询 关于我们
请输入关键词

NSC151098 | 68352-29-4

中文名称
——
中文别名
——
英文名称
NSC151098
英文别名
1-hydroxy-naphthalene-2-carboxylic acid 4-chloro-2-nitro-anilide;4'-Chloro-1-hydroxy-2'-nitro-2-naphthanilide;N-(4-chloro-2-nitrophenyl)-1-hydroxynaphthalene-2-carboxamide
NSC151098化学式
CAS
68352-29-4
化学式
C17H11ClN2O4
mdl
——
分子量
342.738
InChiKey
VYLPTAIYPFRUCX-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):
    5.2
  • 重原子数:
    24
  • 可旋转键数:
    2
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    95.2
  • 氢给体数:
    2
  • 氢受体数:
    4

反应信息

  • 作为反应物:
    描述:
    NSC151098四氢呋喃 以80%的产率得到
    参考文献:
    名称:
    DUBEY S. K.; SINGH A. K.; SINGH H.; SHARMA S.; IYER R. N.; KATIYAR J. C.;+, J. MED. CHEM., 1978, 21, NO 11, 1178-1181
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    DUBEY S. K.; SINGH A. K.; SINGH H.; SHARMA S.; IYER R. N.; KATIYAR J. C.;+, J. MED. CHEM., 1978, 21, NO 11, 1178-1181
    摘要:
    DOI:
点击查看最新优质反应信息

文献信息

  • Synthesis of substituted 1-hydroxy-2-naphthanilides as potential cestodicidal agents
    作者:S. K. Dubey、A. K. Singh、H. Singh、S. Sharma、R. N. Iyer、J. C. Katiyar、P. Goel、A. B. Sen
    DOI:10.1021/jm00209a020
    日期:1978.11
    A series of substituted 1-hydroxy-2-naphthanilides 4--14 has been synthesized by treating 1-hydroxy-2-naphthoic acids 2 with substituted anilines 3. The nitronaphthanilides, on reduction and subsequent treatment with thiophosgene, gave the corresponding substituted 2-naphthanilide isothiocyanates 30--33. Substitution of the chlorine of 8 by various cyclic amines gave 3'-nitro-4'-substituted 1-hydroxy-2-naphthanilides 15--21. Various 3-aryl-4-oxo-2,3-dihydro-1,3-naphthoxazine-2-thiones 34-43 and 3 aryl-2,4-dioxo-2,3-dihydro-1,3-naphthoxazines 44--51 have been prepared by reacting the corresonding naphthanilides with thiophosgene and ethyl chloroformate, respectively. All the compounds were tested for their cestodicidal activity against Hymenolepis nana infection in rats; 30 was found to be the most active compound of the series, showing 100% clearance of infection at a single oral dose of 7.5 mg/kg.
  • DUBEY S. K.; SINGH A. K.; SINGH H.; SHARMA S.; IYER R. N.; KATIYAR J. C.;+, J. MED. CHEM., 1978, 21, NO 11, 1178-1181
    作者:DUBEY S. K.、 SINGH A. K.、 SINGH H.、 SHARMA S.、 IYER R. N.、 KATIYAR J. C.、+
    DOI:——
    日期:——
查看更多