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2-hydroxy-N'-[(4-oxo-4H-chromen-3-yl)methylidene]benzohydrazide

中文名称
——
中文别名
——
英文名称
2-hydroxy-N'-[(4-oxo-4H-chromen-3-yl)methylidene]benzohydrazide
英文别名
2-hydroxy-N-[(4-oxochromen-3-yl)methylideneamino]benzamide
2-hydroxy-N'-[(4-oxo-4H-chromen-3-yl)methylidene]benzohydrazide化学式
CAS
——
化学式
C17H12N2O4
mdl
——
分子量
308.293
InChiKey
WAFYGXXLTQAURQ-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):
    2.9
  • 重原子数:
    23
  • 可旋转键数:
    3
  • 环数:
    3.0
  • sp3杂化的碳原子比例:
    0.0
  • 拓扑面积:
    88
  • 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:
    2-hydroxy-N'-[(4-oxo-4H-chromen-3-yl)methylidene]benzohydrazide三溴化磷三乙胺 作用下, 以 1,4-二氧六环 为溶剂, 反应 10.0h, 以75%的产率得到3-{[(2,4-dioxo-3,4-dihydro-2H-1,3,2λ5-benzoxazaphosphinin-3-yl)imino]methyl}-4H-chromen-4-one
    参考文献:
    名称:
    2-羟基-N'-[(4-氧代-4 H-铬-3-基)亚甲基]苯并肼与某些磷试剂的反应。带有色酮环的新型α-肼基膦酸,1,4,5,2λ5-恶二氮膦和1,3,2λ5-苯并氮杂膦酸的合成及抗癌活性
    摘要:
    新颖1,4,5,2-Oxadiazaphosphinines,1,3,2- benzoxazaphosphinines,和α-hydrazinophosphonic酸轴承色酮环是由2-羟基反应得到Ñ ' - [(4-氧代-4- ħ -色烯-3-基)-亚甲基]苯并肼与某些磷试剂,例如膦酸及其酯,硫化磷和卤化磷。评价合成的化合物对四种癌细胞系的抗癌活性。两种化合物对MCF-7乳腺癌细胞和VEGF抑制表达表现出很高的作用。
    DOI:
    10.1134/s107042801706015x
  • 作为产物:
    描述:
    水杨酰肼色酮-3-甲醛乙醇 为溶剂, 反应 0.5h, 以77%的产率得到2-hydroxy-N'-[(4-oxo-4H-chromen-3-yl)methylidene]benzohydrazide
    参考文献:
    名称:
    2-羟基-N'-[(4-氧代-4 H-铬-3-基)亚甲基]苯并肼与某些磷试剂的反应。带有色酮环的新型α-肼基膦酸,1,4,5,2λ5-恶二氮膦和1,3,2λ5-苯并氮杂膦酸的合成及抗癌活性
    摘要:
    新颖1,4,5,2-Oxadiazaphosphinines,1,3,2- benzoxazaphosphinines,和α-hydrazinophosphonic酸轴承色酮环是由2-羟基反应得到Ñ ' - [(4-氧代-4- ħ -色烯-3-基)-亚甲基]苯并肼与某些磷试剂,例如膦酸及其酯,硫化磷和卤化磷。评价合成的化合物对四种癌细胞系的抗癌活性。两种化合物对MCF-7乳腺癌细胞和VEGF抑制表达表现出很高的作用。
    DOI:
    10.1134/s107042801706015x
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文献信息

  • Activity of some 3-formylchromone derivatives on the induction of chloroplast-free mutants in Euglena gracilis
    作者:Pavlı́na Foltı́nová、Margita Lácová、Dušan Loos
    DOI:10.1016/s0014-827x(99)00114-7
    日期:2000.1
    The hereditary bleaching test on Euglena gracilis was used for detecting extranuclear mutations. The highest bleaching activity (induction of the chloroplast-free mutants) was shown by the 6-R-3-formylchromones. On the other hand, bleaching-inactive 6-R-3-formylchromone acylhydrazones (derived from gallic and salicylic acids), added at sufficient concentrations in the case of chloroplast mutagenesis in E. gracilis, act as a potent antimutagen. This effect appeared to be a unique feature of chromone derivatives, but was dependent on the type of mutagen. These substances were very effective against the bleaching activity of acridine orange, and were less effective against N-methyl-N'-nitro-N-nitrosoguanidine. The genotoxic effects of these mutagens was reduced, especially during the first stages of induction of this specific cytoplasmic mutation. The experimental study of mutagenicity and antimutagenicty of 3-formylchromone hydrazones was reinforced by data obtained by the semi-empirical AM1 method and lipophilicity values. (C) 2000 Elsevier Science S.A. All rights reserved.
  • Synthesis, antimicrobial activity and bleaching effect of some reaction products of 4-oxo-4H-benzopyran-3-carboxaldehydes with aminobenzothiazoles and hydrazides
    作者:Hafez M. El-Shaaer、Pavlína Foltínová、Margita Lácová、Jarmila Chovancová、Henrieta Stankovičová
    DOI:10.1016/s0014-827x(98)00015-9
    日期:1998.3
    The synthesis of the biologically active novel systems derived from reaction of 3-formylchromones with three types of amino derivatives, 6-R-2-2-aminobenzothiazoles, 6-amino-2-R-3-thiobenzothiazoles and hydrazide derivatives (derived from cyanoacetic, isonicotine, salicylic and gallic acids) was carried out. The structures of the prepared compounds have been proved by elemental analysis, H-1 NMR and IR spectra. Antimicrobial activity was studied against the following microorganisms-bacteria G(+) (Staphylococcus aureus 29/58, Bacillus subtilis 18/66), G(-) (Escherichia coli 326/71, Pseudomonas aeruginosa); yeasts: Candida albicans, Saccharomyces cerevisiae; moulds: Microsporum gypseum, Aspergillus niger, Scopulariopsis brevicaulis; and against typical and atypical mycobacteria: Mycobacterium tuberculosis (H37Rv), Mycobacterium kansasii (PFG8), Mycobacterium avium (My 80/72), Mycobacterium fortuitum (1021). The hereditary bleaching effect on the plastid system of Euglena gracilis, a unique phenomenon of the biological activity of chromone derivatives, is reported. The bleaching test on E. gracilis is used for detecting extranuclear mutations. (C) 1998 Elsevier Science S.A. All rights reserved.
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