4-Nitronaphthalene-1-diazonium chloride | 68905-59-9

• 分子结构分类: 有机化合物 - 苯类化合物 - 萘
• 英文名称: 4-Nitronaphthalene-1-diazonium chloride
• 英文别名: 4-nitronaphthalene-1-diazonium;chloride
• CAS: 68905-59-9
• 化学式: C₁₀H₆N₃O₂*Cl
• 分子量: 235.63
• InChiKey: LTZMYEMRABQPOO-UHFFFAOYSA-M

计算性质

• 辛醇/水分配系数(LogP)：
  0.24
• 重原子数：
  16
• 可旋转键数：
  0
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  74
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4-Nitronaphthalene-1-diazonium chloride 、 potassium thioacyanate 在 sodium acetate 作用下， 以 水 为溶剂， 生成 1-Nitro-4-thiocyanato-naphthalin
  参考文献：
  名称：

  Synthesis of some new 5-substituted 1H-tetrazoles

  摘要：

  4-Substituted 1-naphthyl selenocyanates and thiocyanates, as well as 2-naphthyl selenocyanate, were synthesized from the corresponding naphthylamines and were converted into 5-naphthyl-1H-tetrazoles by treatment with sodium azide in the presence of triethylamine hydrochloride in toluene. The structure of the newly synthesized compounds was confirmed by IR, (1)H NMR, and mass spectra.

  DOI：

  10.1134/s1070428009010217
• 作为产物：
  描述：

  1-氨基-4-硝基萘 在 盐酸 、 sodium nitrite 作用下， 以 水 为溶剂， 反应 0.5h， 生成 4-Nitronaphthalene-1-diazonium chloride
  参考文献：
  名称：

  Synthesis of some new 5-substituted 1H-tetrazoles

  摘要：

  4-Substituted 1-naphthyl selenocyanates and thiocyanates, as well as 2-naphthyl selenocyanate, were synthesized from the corresponding naphthylamines and were converted into 5-naphthyl-1H-tetrazoles by treatment with sodium azide in the presence of triethylamine hydrochloride in toluene. The structure of the newly synthesized compounds was confirmed by IR, (1)H NMR, and mass spectra.

  DOI：

  10.1134/s1070428009010217

文献信息

• US4276363A
  申请人：——

  公开号：US4276363A

  公开（公告）日：1981-06-30
• Synthesis of some new 5-substituted 1H-tetrazoles
  作者：A. Dişli、M. Salman

  DOI：10.1134/s1070428009010217

  日期：2009.1

  4-Substituted 1-naphthyl selenocyanates and thiocyanates, as well as 2-naphthyl selenocyanate, were synthesized from the corresponding naphthylamines and were converted into 5-naphthyl-1H-tetrazoles by treatment with sodium azide in the presence of triethylamine hydrochloride in toluene. The structure of the newly synthesized compounds was confirmed by IR, (1)H NMR, and mass spectra.