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N'-(4-nitrobenzylidene)-2-(2-isopropyl-5-methylphenoxy) acetohydrazide | 99004-38-3

中文名称
——
中文别名
——
英文名称
N'-(4-nitrobenzylidene)-2-(2-isopropyl-5-methylphenoxy) acetohydrazide
英文别名
2-(5-methyl-2-propan-2-ylphenoxy)-N-[(4-nitrophenyl)methylideneamino]acetamide
N'-(4-nitrobenzylidene)-2-(2-isopropyl-5-methylphenoxy) acetohydrazide化学式
CAS
99004-38-3
化学式
C19H21N3O4
mdl
——
分子量
355.393
InChiKey
AJWKLOMLVPXTLC-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):
    4.2
  • 重原子数:
    26
  • 可旋转键数:
    6
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.26
  • 拓扑面积:
    96.5
  • 氢给体数:
    1
  • 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:
    硫代乳酸N'-(4-nitrobenzylidene)-2-(2-isopropyl-5-methylphenoxy) acetohydrazide 为溶剂, 反应 6.0h, 以56%的产率得到2-(4-nitrophenyl)-3-(2'-isopropyl-5'-methylphenoxyacetylamino)-5-methyl-4-thiazolidinone
    参考文献:
    名称:
    Roda, K. P.; Vansdadia, R. N.; Parekh, Hansa, Journal of the Indian Chemical Society, 1986, vol. 63, p. 594 - 595
    摘要:
    DOI:
  • 作为产物:
    描述:
    参考文献:
    名称:
    Synthesis and Biological Evaluation of Thymol Functionalized Oxadiazole thiol, Triazole thione and β-lactam Derivatives
    摘要:
    在本研究中,合成了百里香酚(1)的不同衍生物,包括酰肼(2)、噁二唑硫醇(3)、三唑硫酮(4)、腙(5-7)以及β-内酰胺(8-10)。所有合成的化合物均通过元素分析、紫外-可见光谱、1H核磁共振、13C核磁共振和红外光谱技术进行了鉴定和表征。合成的百里香酚衍生物在抑制玉米病原真菌串珠镰刀菌(Fusarium moniliforme)、立枯丝核菌(Rhizoctonia solani)和德雷斯勒霉(Dreschleramaydis)的抗真菌潜力方面与推荐标准进行了比较,涉及抑制百分比和ED50值。百里香酚对所有三种测试的真菌的效力均高于其衍生物。含有间位硝基取代苯环(6, 9)的腙(5-7)和β-内酰胺(8-10)对串珠镰刀菌和立枯丝核菌的效力低于邻位和对位硝基类似物,然而,对德雷斯勒霉的情况则相反。百里香酚及其衍生物还对储存谷物(鹰嘴豆)害虫绿豆象(Callosobruchus chinensis)的杀虫活性进行了测试,并记录和比较了产卵、成虫羽化和谷物损害等参数。含有噁二唑硫醇(3)和三唑硫酮(4)基团的化合物对绿豆象显示出有前景的效果。
    DOI:
    10.2174/1570178617999200807213410
点击查看最新优质反应信息

文献信息

  • Bhat, K. Ishwar; Jainey, Indian Journal of Heterocyclic Chemistry, 2014, vol. 24, # 1, p. 81 - 86
    作者:Bhat, K. Ishwar、Jainey
    DOI:——
    日期:——
  • Roda, K. P.; Vansdadia, R. N.; Parekh, Hansa, Journal of the Indian Chemical Society, 1986, vol. 63, p. 594 - 595
    作者:Roda, K. P.、Vansdadia, R. N.、Parekh, Hansa
    DOI:——
    日期:——
  • Synthesis and Biological Evaluation of Thymol Functionalized Oxadiazole thiol, Triazole thione and β-lactam Derivatives
    作者:Jyoti Gaba、Sunita Sharma、Pardeep Kaur、Sukesha Joshi
    DOI:10.2174/1570178617999200807213410
    日期:2021.6
    <p>In the present study, different derivatives of thymol (1) viz. hydrazide (2), oxadiazole thiol (3), triazole thione (4), hydrazones (5-7), and &#946;-lactams (8-10) were synthesized. All synthesized compounds were identified and characterized using elemental analysis, UV-Visible, <sup>1</sup>H NMR, <sup>13</sup>C NMR, and IR spectroscopic techniques. Synthesized thymol derivatives were evaluated for antifungal potential against phytopathogenic fungi Fusarium moniliforme, Rhizoctonia solani, and Dreschlera maydis of maize in comparison to recommended standards in terms of percent inhibition and ED50 values. Thymol was more effective as compared to its derivatives against all three tested fungi. Hydrazones (5-7) and &#946;-lactams (8-10), having m-NO<sub>2</sub> substituted phenyl ring (6, 9), were less effective as compared to o-NO<sub>2</sub> and p-NO<sub>2</sub> analogs against F. moniliforme and R. solani, however, the reverse trend was observed against D. maydis. Thymol and its derivatives were also tested for insecticidal activity against stored grain (chickpea) insect Callosobruchus chinensis and various parameters viz. egg laying, adult emergence, and grain damage were recorded and compared. Compounds having oxadiazole thiol (3) and triazole thione (4) moiety showed promising effects against insect C. chinensis.</p> </sec></div> <div class="value-text ch">在本研究中,合成了百里香酚(1)的不同衍生物,包括酰肼(2)、噁二唑硫醇(3)、三唑硫酮(4)、腙(5-7)以及&#946;-内酰胺(8-10)。所有合成的化合物均通过元素分析、紫外-可见光谱、<sup>1</sup>H核磁共振、<sup>13</sup>C核磁共振和红外光谱技术进行了鉴定和表征。合成的百里香酚衍生物在抑制玉米病原真菌串珠镰刀菌(Fusarium moniliforme)、立枯丝核菌(Rhizoctonia solani)和德雷斯勒霉(Dreschleramaydis)的抗真菌潜力方面与推荐标准进行了比较,涉及抑制百分比和ED50值。百里香酚对所有三种测试的真菌的效力均高于其衍生物。含有间位硝基取代苯环(6, 9)的腙(5-7)和&#946;-内酰胺(8-10)对串珠镰刀菌和立枯丝核菌的效力低于邻位和对位硝基类似物,然而,对德雷斯勒霉的情况则相反。百里香酚及其衍生物还对储存谷物(鹰嘴豆)害虫绿豆象(Callosobruchus chinensis)的杀虫活性进行了测试,并记录和比较了产卵、成虫羽化和谷物损害等参数。含有噁二唑硫醇(3)和三唑硫酮(4)基团的化合物对绿豆象显示出有前景的效果。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=30fd5e7r3e6d938151N0&inchikey=AJWKLOMLVPXTLC-UHFFFAOYSA-N" target="_blank" rel="nofollow" class="view-more">查看更多</a> </div> <div class="module" id="tongleihuahewu"> <h3 class="module-title"><i class="iconfont 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href="https://www.molaid.com/fenzi/24" class="compound-item" title="有机聚合物">有机聚合物</a> <a href="https://www.molaid.com/fenzi/25" class="compound-item" title="有机金属化合物">有机金属化合物</a> <a href="https://www.molaid.com/fenzi/26" class="compound-item" title="乙炔化物 ">乙炔化物 </a> <a href="https://www.molaid.com/fenzi/27" class="compound-item" title="有机磷化合物">有机磷化合物</a> <a href="https://www.molaid.com/fenzi/28" class="compound-item" title="叠烯">叠烯</a> <a href="https://www.molaid.com/fenzi/29" class="compound-item" title="有机1,3-偶极化合物">有机1,3-偶极化合物</a> <a href="https://www.molaid.com/fenzi/30" class="compound-item" title="碳化物">碳化物</a> <a href="https://www.molaid.com/fenzi/31" class="compound-item" title="有机盐">有机盐</a> <a href="https://www.molaid.com/fenzi/32" class="compound-item" title="有机阳离子">有机阳离子</a> <a href="https://www.molaid.com/fenzi/33" class="compound-item" title="卡宾">卡宾</a> <a href="https://www.molaid.com/fenzi/34" class="compound-item" title="有机阴离子">有机阴离子</a> </div> </div> </div> <div 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" 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