2-(4-甲基苯氧基)丙肼 | 83798-16-7

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯酚醚
• 中文名称: 2-(4-甲基苯氧基)丙肼
• 中文别名: 2-(4-甲基苯氧基)丙烷肼
• 英文名称: 2-(4-Methylphenoxy)propanohydrazide
• 英文别名: 2-(4-methylphenoxy)propanehydrazide
• CAS: 83798-16-7
• 化学式: C₁₀H₁₄N₂O₂
• mdl: MFCD02269956
• 分子量: 194.233
• InChiKey: VLEDMATYRJUZNS-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.3
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.3
• 拓扑面积：
  64.4
• 氢给体数：
  2
• 氢受体数：
  3

安全信息

• 危险等级：
  IRRITANT
• 危险品标志：
  Xi
• 海关编码：
  2928000090

反应信息

• 作为反应物：
  描述：

  2-(4-甲基苯氧基)丙肼 在 氢氧化钾 作用下， 以 甲醇 为溶剂， 反应 9.0h， 生成 5-[1-(4-methylphenoxy)ethyl]-3-[[4-[[5-[1-(4-methylphenoxy)ethyl]-2-sulfanylidene-1,3,4-oxadiazol-3-yl]methyl]piperazin-1-yl]methyl]-1,3,4-oxadiazole-2-thione
  参考文献：
  名称：

  Mishra, Vinod Kumar; Bahel, Suresh Chandra, Acta Chimica Hungarica, 1984, vol. 117, # 4, p. 357 - 362

  摘要：

  DOI：
• 作为产物：
  描述：

  2-(4-甲基苯氧基)丙酸乙酯 在 肼 作用下， 生成 2-(4-甲基苯氧基)丙肼
  参考文献：
  名称：

  新型含二酰基肼/ 1,3,4-Oxadiazole部分的N-吡啶基吡唑衍生物的合成和杀虫作用评估

  摘要：

  两个系列新颖的Ñ含二酰基肼/ 1,3,4-恶二唑基部分-pyridylpyrazole衍生物，设计并基于氯虫苯甲酰胺的结构和特征的合成通过 1 H-NMR，13 C-NMR，IR，MS和元素分析。初步的生物测定表明，某些标题化合物I和II对Mythimna separata表现出杀幼虫活性，在500 mg / L时死亡率为90-100％。进一步测试表明，这些化合物对Mythimna separata和Plutella xylostella的杀虫活性较弱。 浓度为200 mg / L，可能不适合用作进一步优化的杀虫剂铅化合物。

  DOI：

  10.1002/jhet.3505

文献信息

• Studies on 1,2,4-Triazole Derivatives as Potential Anti-Inflammatory Agents
  作者：Gülhan Turan-Zitouni、Zafer Asim Kaplancikli、Ahmet Özdemir、Pierre Chevallet、Hilmi Burak Kandilci、Bülent Gümüsel

  DOI：10.1002/ardp.200700134

  日期：2007.11

  4‐aryl/alkyl‐5‐(1‐phenoxyethyl)‐3‐[N‐(substituted)acetamido]thio‐4H‐1,2,4‐triazole derivatives were synthesized by reacting the triazoles with 2‐chloro‐N‐(substituted)acetamide. The chemical structures of the compounds were elucidated by IR, 1H‐NMR, FAB+‐MS spectral data and elemental analysis. In the pharmacological studies, anti‐inflammatory activities of these compounds have been screened and significant

  乙酸或丙酸酰肼与各种芳基/烷基异硫氰酸酯反应生成缩氨基硫脲，通过碱环化得到1,2,4-三唑。4-芳基/烷基-5-(1-苯氧基乙基)-3-[N-(取代)乙酰氨基]硫代-4H-1,2,4-三唑衍生物通过三唑与2-氯-N-反应合成（取代的）乙酰胺。化合物的化学结构经IR、1H-NMR、FAB+-MS谱数据和元素分析阐明。在药理研究中，已筛选出这些化合物的抗炎活性并观察到显着的活性。
• Synthesis and antimicrobial activity of 4-phenyl/cyclohexyl-5-(1-phenoxyethyl)-3-[N-(2-thiazolyl)acetamido]thio-4H-1,2,4-triazole derivatives
  作者：Gülhan Turan-Zitouni、Zafer Asım Kaplancıklı、Mehmet Taha Yıldız、Pierre Chevallet、Demet Kaya

  DOI：10.1016/j.ejmech.2005.01.007

  日期：2005.6

  drug-resistant fungal and bacterial pathogens has lent additional urgency to microbiological research and new antimicrobial compound development. For this purpose, new thiazole derivatives of triazoles were synthesized and evaluated for antifungal and antibacterial activity. The reaction of propionic acid hydrazides with various aryl/alkyl isothiocyanates gave thiosemicarbazides which furnished the

  耐药真菌和细菌病原体的临床重要性日益提高，这为微生物学研究和新的抗菌化合物的开发提供了额外的紧迫性。为此目的，合成了新的三唑噻唑衍生物并评估了其抗真菌和抗菌活性。丙酸酰肼与各种芳基/烷基异硫氰酸酯的反应得到硫代氨基脲，其通过碱环化得到巯基三唑。通过使巯基三唑与2-氯-环己基反应合成4-苯基/环己基-5-（1-苯氧基乙基）-3- [N-（2-噻唑基）乙酰胺基]硫基-4H-1,2,4-三唑衍生物。 N-（2-噻唑基）乙酰胺。通过IR，1 H-NMR，FAB + -MS光谱数据阐明了化合物的化学结构。它们对白色念珠菌（两种菌株）具有抗菌活性，调查了光滑念珠菌，大肠杆菌，金黄色葡萄球菌，铜绿假单胞菌。结果表明，某些化合物具有很强的抗真菌活性。
• Pathak; Srivastava; Bahel, Journal of the Indian Chemical Society, 1982, vol. 59, # 6, p. 776 - 778
  作者：Pathak、Srivastava、Bahel

  DOI：——

  日期：——
• Turan-Zitouni; Kaplancikli; Guven, Il Farmaco, 1997, vol. 52, # 10, p. 631 - 633
  作者：Turan-Zitouni、Kaplancikli、Guven

  DOI：——

  日期：——
• A Facile One-Pot Synthesis of 2-Arylamino-5-Aryloxylalkyl-1,3,4-Oxadiazoles and Their Urease Inhibition Studies
  作者：Tashfeen Akhtar、Muhammad A. Khan、Jamshed Iqbal、Peter G. Jones、Shahid Hameed

  DOI：10.1111/cbdd.12297

  日期：2014.7

  A one‐pot method for the synthesis of structural type urease inhibitors, 2‐amino‐1,3,4‐oxadiazoles, was developed. The structures of the compounds were established using spectroanalytical techniques and unambiguously confirmed by single‐crystal X‐ray analysis of compound 3o. The synthesized compounds were tested against jack beans urease, and most of the compounds (3c, 3g, 3j, 3k, 3n, 3r–3v) were found more active than the standard. The most potent compound (3u) had an IC50 value of 6.03 ± 0.02 μm as compared to the IC50 value of the standard (thiourea; 22.0 ± 1.2 μm). The prominent urease inhibition activity of these compounds may serve as an important finding in the development of less toxic and more potent antiulcer drugs. The compounds were also investigated against four bacterial strains, and some of the compounds (3g and 3r) were found more potent than the standard drug (ciprofloxacin) against all the tested strains. The MIC value for compound 3g was 0.156 μmol/mL against the tested bacterial strains.