3-(2-benzoxazolylthio)propanenitrile | 25176-73-2

• 分子结构分类: 有机化合物 - 有机杂环化合物 - 苯并恶唑类
• 英文名称: 3-(2-benzoxazolylthio)propanenitrile
• 英文别名: 3-(2-Benzoxazolylthio)propionitrile；3-(1,3-benzoxazol-2-ylsulfanyl)propanenitrile
• CAS: 25176-73-2
• 化学式: C₁₀H₈N₂OS
• mdl: MFCD01575204
• 分子量: 204.252
• InChiKey: UMTKYUOKOWVCCI-UHFFFAOYSA-N

物化性质

• 熔点：
  45-46 °C
• 沸点：
  386.7±44.0 °C(Predicted)
• 密度：
  1.30±0.1 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.4
• 重原子数：
  14
• 可旋转键数：
  3
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  75.1
• 氢给体数：
  0
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  3-(2-benzoxazolylthio)propanenitrile 在 盐酸 作用下， 以90%的产率得到3-(2-Benzoxazolylthio)propionic acid
  参考文献：
  名称：

  Benzazolin-2-thiones in the michael reaction. 1. Reaction of benzothiazolin- and benzoxazolin-2-thiones with acrylonitrile, acrylamide, and methylacrylate in the presence of acid catalysts

  摘要：

  DOI：

  10.1007/bf00542791
• 作为产物：
  描述：

  3-(2-Benzoxazolylthio)propionamide 在 N,N-二甲基甲酰胺 、 三氯氧磷 作用下， 反应 1.0h， 以86%的产率得到3-(2-benzoxazolylthio)propanenitrile
  参考文献：
  名称：

  D'Amico, John J.; Suba, Lydia; Ruminski, Peter G., Journal of Heterocyclic Chemistry, 1986, vol. 23, p. 1629 - 1635

  摘要：

  DOI：

文献信息

• 3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives: inhibitors of immune complex induced inflammation
  作者：Fortuna Haviv、James D. Ratajczyk、Robert W. DeNet、Francis A. Kerdesky、Roland L. Walters、Steven P. Schmidt、James H. Holms、Patrick R. Young、George W. Carter

  DOI：10.1021/jm00117a010

  日期：1988.9

  3-[1-(2-Benzoxazolyl)hydrazino]propanenitrile derivatives were evaluated in the dermal and pleural reverse passive Arthus reactions in the rat. In the pleural test these compounds were effective in reducing exudate volume and accumulation of white blood cells. This pattern of activity was similar to that of hydrocortisone and different from that of indomethacin. The structural requirements for inhibiting the Arthus reactions were studied by systematic chemical modification of 1. These structure-activity relationship studies revealed that nitrogen 1' of the hydrazino group is essential for activity and must be electron rich, whereas chemical modifications of other sites of 1 had only a modest effect on activity.
• An easy and fast ultrasonic selective S-alkylation of hetaryl thiols at room temperature
  作者：Todor Deligeorgiev、Stefka Kaloyanova、Nedyalko Lesev、Juan J. Vaquero

  DOI：10.1016/j.ultsonch.2010.03.002

  日期：2010.6

  A series of 2-alkylthio derivatives of hetaryl thiols were synthesized by selective S-alkylation with alkyl halides (bromides and iodides) with ultrasonic irradiation at room temperature. The reaction was found to be generally applicable to hetaryl thiol derivatives with different substituents in the aromatic nucleus and various alkyl halides. The reaction gives high to excellent yields of products with high purity. (C) 2010 Elsevier B.V. All rights reserved.
• HAVIV, FORTUNA;RATAJCZYK, JAMES D.;DENET, ROBERT W.;KERDESKY, FRANCIS A.;+, J. MED. CHEM., 31,(1988) N 9, C. 1719-1728
  作者：HAVIV, FORTUNA、RATAJCZYK, JAMES D.、DENET, ROBERT W.、KERDESKY, FRANCIS A.、+

  DOI：——

  日期：——
• D'Amico, John J.; Suba, Lydia; Ruminski, Peter G., Journal of Heterocyclic Chemistry, 1986, vol. 23, p. 1629 - 1635
  作者：D'Amico, John J.、Suba, Lydia、Ruminski, Peter G.

  DOI：——

  日期：——
• Benzazolin-2-thiones in the michael reaction. 1. Reaction of benzothiazolin- and benzoxazolin-2-thiones with acrylonitrile, acrylamide, and methylacrylate in the presence of acid catalysts
  作者：K. V. Anan'eva、N. K. Rozhkov

  DOI：10.1007/bf00542791

  日期：1986.4