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4,9-dihydro-4,9-dioxo-6-hydroxy-1H-naphtho[2,3-d]-v-triazole | 80841-85-6

中文名称
——
中文别名
——
英文名称
4,9-dihydro-4,9-dioxo-6-hydroxy-1H-naphtho[2,3-d]-v-triazole
英文别名
6-hydroxy-2H-benzo[f]benzotriazole-4,9-dione
4,9-dihydro-4,9-dioxo-6-hydroxy-1H-naphtho[2,3-d]-v-triazole化学式
CAS
80841-85-6
化学式
C10H5N3O3
mdl
——
分子量
215.168
InChiKey
UUHBYBMYCKYIJR-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

  • 熔点:
    285 °C (decomp)
  • 沸点:
    525.8±40.0 °C(Predicted)
  • 密度:
    1.759±0.06 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    0.9
  • 重原子数:
    16
  • 可旋转键数:
    0
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    95.9
  • 氢给体数:
    2
  • 氢受体数:
    5

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

  • 作为反应物:
    描述:
    乙酸酐4,9-dihydro-4,9-dioxo-6-hydroxy-1H-naphtho[2,3-d]-v-triazole 反应 0.5h, 以55%的产率得到6-acetoxy-4,9-dihydro-4,9-dioxo-1H-naphtho[2,3-d]-v-triazole
    参考文献:
    名称:
    Studies on v-triazoles. 9. Antiallergic 4,9-dihydro-4,9-dioxo-1H-naphtho[2,3-d]-v-triazoles
    摘要:
    A short series of the title compounds was prepared and evaluated for antiallergic activity in the rat passive cutaneous anaphylaxis screen. All but the two N-methylated derivatives were active in this screen by the intravenous route, the most potent being the symmetrical dimethyl compound, 4,9-dihydro-6,7-dimethyl-4,9-dioxo-1H-naphtho[2,3-d]-v-triazole, and its 5-nitro derivative. The latter two compounds were noticeably more potent than disodium cromoglycate, and one of these, the unnitrated material, was selected for further evaluation as a potential antiasthmatic drug.
    DOI:
    10.1021/jm00359a016
  • 作为产物:
    参考文献:
    名称:
    Studies on v-triazoles. 9. Antiallergic 4,9-dihydro-4,9-dioxo-1H-naphtho[2,3-d]-v-triazoles
    摘要:
    A short series of the title compounds was prepared and evaluated for antiallergic activity in the rat passive cutaneous anaphylaxis screen. All but the two N-methylated derivatives were active in this screen by the intravenous route, the most potent being the symmetrical dimethyl compound, 4,9-dihydro-6,7-dimethyl-4,9-dioxo-1H-naphtho[2,3-d]-v-triazole, and its 5-nitro derivative. The latter two compounds were noticeably more potent than disodium cromoglycate, and one of these, the unnitrated material, was selected for further evaluation as a potential antiasthmatic drug.
    DOI:
    10.1021/jm00359a016
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文献信息

  • TEDDER, J. M.;BUCKLE, D. R., J. CHEM. RES. SYNOP., 1983, N 1, 12-13
    作者:TEDDER, J. M.、BUCKLE, D. R.
    DOI:——
    日期:——
  • BUCKLE, D. R.;SMITH, H.;SPICER, B. A.;TEDDER, J. M., J. MED. CHEM., 1983, 26, N 5, 714-719
    作者:BUCKLE, D. R.、SMITH, H.、SPICER, B. A.、TEDDER, J. M.
    DOI:——
    日期:——
  • Studies on v-triazoles. 9. Antiallergic 4,9-dihydro-4,9-dioxo-1H-naphtho[2,3-d]-v-triazoles
    作者:Derek R. Buckle、Harry Smith、Barbara A. Spicer、John Martin Tedder
    DOI:10.1021/jm00359a016
    日期:1983.5
    A short series of the title compounds was prepared and evaluated for antiallergic activity in the rat passive cutaneous anaphylaxis screen. All but the two N-methylated derivatives were active in this screen by the intravenous route, the most potent being the symmetrical dimethyl compound, 4,9-dihydro-6,7-dimethyl-4,9-dioxo-1H-naphtho[2,3-d]-v-triazole, and its 5-nitro derivative. The latter two compounds were noticeably more potent than disodium cromoglycate, and one of these, the unnitrated material, was selected for further evaluation as a potential antiasthmatic drug.
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