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1-(2,4-dinitrophenyl)-3,5-dimethylpyrazole | 7474-11-5

中文名称
——
中文别名
——
英文名称
1-(2,4-dinitrophenyl)-3,5-dimethylpyrazole
英文别名
1‐(2,4‐dinitrophenyl)‐3,5‐dimethyl‐1H‐pyrazole;1-(2,4-dinitro-phenyl)-3,5-dimethyl-1H-pyrazole;1-(2,4-dinitrophenyl)-3,5-dimethyl-1H-pyrazole;1-(2',4'-dinitrophenyl)-3-5-dimethylpyrazole;N-(2',4'-dinitrophenyl)-3,5-dimethylpyrazole;1-(2,4-dinitro-phenyl)-3,5-dimethyl-1H-pyrazole
1-(2,4-dinitrophenyl)-3,5-dimethylpyrazole化学式
CAS
7474-11-5
化学式
C11H10N4O4
mdl
MFCD00020723
分子量
262.225
InChiKey
UMBVNCGCAYHVJO-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:
    122 °C
  • 沸点:
    418.6±45.0 °C(Predicted)
  • 密度:
    1.47±0.1 g/cm3(Predicted)

计算性质

  • 辛醇/水分配系数(LogP):
    2.3
  • 重原子数:
    19
  • 可旋转键数:
    1
  • 环数:
    2.0
  • sp3杂化的碳原子比例:
    0.18
  • 拓扑面积:
    110
  • 氢给体数:
    0
  • 氢受体数:
    5

SDS

SDS:25354a1b765f0cf6df95ab15e36364a5
查看

反应信息

  • 作为反应物:
    描述:
    1-(2,4-dinitrophenyl)-3,5-dimethylpyrazole碘苯二乙酸 作用下, 以 二氯甲烷 为溶剂, 反应 0.5h, 以90%的产率得到4-iodo-3,5-dimethyl-1-(2,4-dinitrophenyl)pyrazole
    参考文献:
    名称:
    Hypervalent Iodine in Synthesis. 90. A Mild and Efficient Method for the Iodination of Pyrazoles
    摘要:
    The combined reagent of iodobenzene diacetate (or polymersupported iodobenzene diacetate) with iodine was used as an effective iodinating agent of pyrazoles to the corresponding 4-iodopyrazole derivatives at room temperature with high yields.
    DOI:
    10.1081/scc-120021987
  • 作为产物:
    参考文献:
    名称:
    CIII。– 2:4-二硝基苯肼用作羰基化合物的试剂
    摘要:
    DOI:
    10.1039/jr9310000756
点击查看最新优质反应信息

文献信息

  • Cu<sub>1.5</sub> PMo<sub>12</sub> O<sub>40</sub> -catalyzed condensation cyclization for the synthesis of substituted pyrazoles
    作者:Guo-Ping Yang、Xing He、Bing Yu、Chang-Wen Hu
    DOI:10.1002/aoc.4532
    日期:2018.11
    A convenient and direct approach has been developed for the preparation of pyrazole derivatives by the condensation cyclization of hydrazines/hydrazide and 1,3‐diketones in the presence of Cu1.5PMo12O40 (0.33 mol%) under mild conditions (r.t.‐60 °C, 10–30 min). Notably, the reaction was found to be scalable as 99% yield was obtained when the reaction was performed at a 5‐mmol scale. This solvent‐free
    在温和的条件下(rt-60),在Cu 1.5 PMo 12 O 40(0.33 mol%)存在下,通过肼/酰肼和1,3-二酮的缩合环化反应,已经开发了一种方便直接的方法来制备吡唑衍生物。°C,10–30分钟)。值得注意的是,当反应在5 mmol规模下进行时,发现该反应可扩展,产率为99%。这种无溶剂和无卤素的催化体系代表了吡唑的一种有效的经济和环保方法。
  • Efficient Copper-Catalyzed Synthesis of Substituted Pyrazoles at Room Temperature
    作者:Haifeng Wang、Xiangli Sun、Shuangling Zhang、Guanglu Liu、Chunjie Wang、Lili Zhu、Hui Zhang
    DOI:10.1055/s-0037-1610330
    日期:2018.12
    method for the synthesis of pyrazoles through a copper-catalyzed condensation reaction has been developed. The new catalytic system not only maintained a broad substrate scope but was also active under acid-free reaction conditions, overcoming the conventional requirement for an acid-catalyzed system. Furthermore, the copper catalyst enabled this reaction to be performed at room temperature and in a short
    已开发出一种通过铜催化缩合反应合成吡唑的有效方法。新的催化体系不仅保持了广泛的底物范围,而且在无酸反应条件下也具有活性,克服了对酸催化体系的传统要求。此外,铜催化剂使该反应能够在室温下和较短的反应时间内进行。
  • Nano-SnCl4/SiO2 as a Catalyst for One-Pot Synthesis of Substituted 1H-Pyrazoles as Antifungal and Cytotoxic Agents
    作者:Soghra Khabnadideh、Zeinab Faghih、Leila Zamani、Kamiar Zomorodian、Bi Bi Fatemeh Mirjalili、Hadi Moradi
    DOI:10.2174/1570178617666191127104622
    日期:2020.5.20
    <p>A simple and efficient method was developed for the synthesis of pyrazole derivatives via a one-pot reaction of 1,3-diketone and substituted hydrazines in the presence of nano-SnCl4/SiO2 as a mild catalyst. A series of some pyrazole derivatives (P1-P11) was synthesized and evaluated as antifungal and anti-cancer agents. Compounds P10 and P11 were demonstrated. The antimicrobial activities of the synthetic compounds showed that compounds P10 and P11 most excellently inhibited the growth of dermatophytes or Aspergillus species, respectively. Therefore, the cytotoxic activities of these compounds on two human cancer cell lines, A549 (lung cancer) and MCF-7 (breast cancer) were further assessed. Hence, results demonstrated that beside antifungal activity, P10 had also desirable cytotoxic effect on investigated cancerous cell lines, even higher than cisplatin.</p> </sec></div> <div class="value-text ch">通过在存在纳米SnCl4/SiO2作为温和催化剂的条件下,1,3-二酮和取代的肼的一锅法反应合成吡唑衍生物的简单高效方法已经开发。合成了一系列一些吡唑衍生物(P1-P11)并评估其作为抗真菌和抗癌剂的活性。化合物P10和P11被证明具有抗菌活性。合成化合物的抗菌活性显示,化合物P10和P11最有效地抑制了白色念珠菌或曲霉菌的生长。因此,对这些化合物在两种人类癌细胞系A549(肺癌)和MCF-7(乳腺癌)上的细胞毒活性进行了进一步评估。结果表明,除了抗真菌活性外,P10对研究的癌细胞系也具有理想的细胞毒作用,甚至高于顺铂。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">A Modified and Practical Synthetic Route to Indazoles and Pyrazoles Using Tungstate Sulfuric Acid</div> <div class="value"> <div class="value-text"> <span>作者:</span>S. Setareh Rahmatzadeh、Bahador Karami、Saeed Khodabakhshi </div> <div class="value-text"> <span>DOI:</span>10.1002/jccs.201400251 </div> <div class="value-text"> <span>日期:</span>2015.1 </div> <div class="value-text en">Tungstate <span style='color:#ff0000'>sulfuric</span> <span style='color:#ff0000'>acid</span>‐<span style='color:#ff0000'>catalyzed</span> Knorr <span style='color:#ff0000'>reaction</span> have been used as a simple, rapid, atom economic and green method for the <span style='color:#ff0000'>synthesis</span> of indazole and pyrazole derivatives based on the condensation of hydrazine derivatives and ß‐dicarbonyl compounds under solvent‐free conditions. It was found that the catalyst could be recovered and reused without significant loss of its activity. The use of this method</div> <div class="value-text ch">钨酸盐硫酸催化的克诺尔反应是一种简单,快速,原子经济且绿色的方法,该方法以肼衍生物和ß-二羰基化合物在无溶剂条件下的缩合为基础,合成吲唑和吡唑衍生物。发现该催化剂可以回收和再利用而不会显着损失其活性。在干净的反应曲线,使用安全的催化剂和无溶剂的条件方面,该方法的使用为克诺尔合成提供了新颖且改进的修饰。</div> </div> </li> <li class="feature-list-item"> <div class="content-title">A Green Protocol for Catalyst-Free Syntheses of Pyrazole in Glycerol-Water Solution</div> <div class="value"> <div class="value-text"> <span>作者:</span>Zhen-Li Min、Qian Zhang、Xing Hong、Xiao-Lu Cao、Xia-Min Hu </div> <div class="value-text"> <span>DOI:</span>10.14233/ajchem.2015.18394 </div> <div class="value-text"> <span>日期:</span>—— </div> <div class="value-text en">An efficient green protocol for preparing pyrazole derivatives using glycerol and water as a mixture solvent is described. The advantages of the present method lie in using economic and environmentally benign solvent, no use of catalyst, mild reaction conditions and good yields.</div> <div class="value-text ch">介绍了一种使用甘油和水混合溶剂制备吡唑衍生物的高效绿色方案。本方法的优势在于采用了经济环保的溶剂,无需使用催化剂,反应条件温和且产率高。</div> </div> </li> </ul> <a href="https://chem.molaid.com/material/detail?source=UserSourcePortal&id=310192dy0d17198153N0&inchikey=UMBVNCGCAYHVJO-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 icon-tongleihuahewu"></i>同类化合物</h3> <div class="compounds-list"> <a target="_blank" href="https://www.molaid.com/MS_4" class="compound-item" title="伊莫拉明">伊莫拉明</a> <a target="_blank" href="https://www.molaid.com/MS_97" class="compound-item" 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title="有机硫化合物">有机硫化合物</a> <a href="https://www.molaid.com/fenzi/19" class="compound-item" title="核苷、核苷酸和类似物">核苷、核苷酸和类似物</a> <a href="https://www.molaid.com/fenzi/20" class="compound-item" title="碳氢化合物衍生物">碳氢化合物衍生物</a> <a href="https://www.molaid.com/fenzi/21" class="compound-item" title="有机氮化合物">有机氮化合物</a> <a href="https://www.molaid.com/fenzi/22" class="compound-item" title="碳氢化合物">碳氢化合物</a> <a href="https://www.molaid.com/fenzi/23" class="compound-item" title="有机卤素化合物">有机卤素化合物</a> <a 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 class="right"> <div class="module"> <link rel="stylesheet" href="https://www.molaid.com/assets/css/common/hot-molecular.css?v=202504271"> <div class="component-card hot-molecular-card" style="--color: #FF4539;"> <div class="title"> <h3 class="title-name">热门分子</h3> </div> <div class="card-content"> <ul class="list"> <li class="item item-special" data-sort="TOP"> <div class="item-img"> <img src="data:image/svg+xml;base64,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