2-(2-甲基-2-丙烯-1-基)氯苯 | 90794-46-0

• 分子结构分类: 有机化合物 - 苯类化合物 - 苯和取代衍生物
• 中文名称: 2-(2-甲基-2-丙烯-1-基)氯苯
• 英文名称: 1-Chloro-2-(2-methyl-2-propenyl)benzene
• 英文别名: 1-chloro-2-(2-methylallyl)benzene；3-<2-Chlor-phenyl>-isobuten-(1)；3-(2-Chlorophenyl)-2-methyl-1-propene；1-chloro-2-(2-methylprop-2-enyl)benzene
• CAS: 90794-46-0
• 化学式: C₁₀H₁₁Cl
• mdl: MFCD00671895
• 分子量: 166.65
• InChiKey: SNKXIABFGGVLRD-UHFFFAOYSA-N

物化性质

• 沸点：
  215.2±9.0 °C(Predicted)
• 密度：
  1.028±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  4.2
• 重原子数：
  11
• 可旋转键数：
  2
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.2
• 拓扑面积：
  0
• 氢给体数：
  0
• 氢受体数：
  0

安全信息

• 海关编码：
  2903999090

反应信息

• 作为反应物：
  描述：

  2-(2-甲基-2-丙烯-1-基)氯苯 在 硫酸 、 三氯化铁 作用下， 以 二氯甲烷 、 溶剂黄146 为溶剂， 生成
  参考文献：
  名称：

  Synthesis and radical scavenging activity of 3,3-dialkyl-3,4-dihydro-isoquinoline 2-oxides

  摘要：

  The syntheses and antioxidant activities of several cyclic nitrones related to phenyl t-butyl nitrone (PBN) are described. These nitrones may act as radical scavengers and have potential uses in the treatment of stroke and septic shock. (C) 1996 Elsevier Science Ltd

  DOI：

  10.1016/0960-894x(96)00181-3
• 作为产物：
  描述：

  2-溴氯苯 、 3-氯-2-甲基丙烯 生成 2-(2-甲基-2-丙烯-1-基)氯苯
  参考文献：
  名称：

  Ruechardt,C.; Eichler,S., Chemische Berichte, 1962, vol. 95, p. 1921 - 1942

  摘要：

  DOI：

文献信息

• Cross-Coupling Synthesis of Methylallyl Alkenes: Scope Extension and Mechanistic Study
  作者：Clémence Tabélé、Christophe Curti、Youssef Kabri、Nicolas Primas、Patrice Vanelle

  DOI：10.3390/molecules201219886

  日期：——

  Cross-coupling reactions between 2-methyl-2-propen-1-ol and various boronic acids are used to obtain aromatic-(2-methylallyl) derivatives. However, deboronation or isomerization side reactions may occur for several boronic acids. We describe herein the synthesis of original alkenes with good yields under mild reaction conditions that decrease these side reactions. The scope of this environmentally benign reaction is thereby extended to a wide variety of boronic acids. A mechanistic study was conducted and suggested a plausible catalytic cycle mechanism, pointing to the importance of the Lewis acidity of the boronic acid used.

  2-甲基-2-丙烯-1-醇与多种硼酸之间的交叉耦合反应可用于制备芳香性（2-甲基烯丙基）衍生物。然而，某些硼酸可能会发生去硼化或异构化副反应。本文描述了在温和反应条件下，通过降低这些副反应，合成产率良好的原始烯烃的方法。因此，这种环境友好的反应的范围得到了扩展，可涵盖更多种类的硼酸。我们对反应机理进行了研究，并提出了一种可能的催化循环机制，指出了所使用硼酸的Lewis酸性的重要性。
• [EN] COMPOUNDS FOR THE TREATMENT OF BOVINE OR SWINE RESPIRATORY DISEASE<br/>[FR] COMPOSÉS POUR LE TRAITEMENT D'UNE MALADIE RESPIRATOIRE BOVINE OU PORCINE
  申请人：INTERVET INT BV

  公开号：WO2020002238A1

  公开（公告）日：2020-01-02

  The present invention provides compounds of formula (I) for use in the treatment of respiratory diseases of animals, especially Bovine or Swine Respiratory disease (BRD and SRD).

  本发明提供了用于治疗动物呼吸道疾病，特别是牛或猪呼吸道疾病（BRD和SRD）的化合物（I）的公式。
• Tandem cyclization-cycloaddition reaction of rhodium carbenoids. Studies dealing with intramolecular cycloadditions
  作者：Albert Padwa、Susan F. Hornbuckle、Glen E. Fryxell、Zhijia J. Zhang

  DOI：10.1021/jo00047a032

  日期：1992.10

  A series of 5-alkenyl-1-diazo-2,5-pentanediones, when treated with a catalytic quantity of rhodium(II) acetate, were found to give cycloadducts derived from the intramolecular trapping of a carbonyl ylide intermediate. Tethers of three or four methylenes readily enter into intramolecular cycloaddition, while longer and shorter tethers were reluctant to do so. Alkenes attached to the formally cationic terminus of the carbonyl ylide readily undergo internal cycloaddition if the tether allows for a relatively strain-free transition state. The internal cycloaddition reaction does not occur when the olefinic side chain is attached by means of an ester functionality. Bimolecular trapping experiments established that carbonyl ylide formation occurred, but the dipole does not undergo intramolecular cycloaddition. The inability of these alpha-diazo keto esters to undergo internal cycloaddition is related to conformational factors. The equilibrium between the two possible conformations of the dipole lies predominantly on the side of the Z-isomer. In this orientation, intramolecular dipolar cycloaddition cannot occur, and instead the dipole collapses by means of a proton transfer to give an enol ether.
• US7595399B2
  申请人：——

  公开号：US7595399B2

  公开（公告）日：2009-09-29
• Ruechardt,C.; Eichler,S., Chemische Berichte, 1962, vol. 95, p. 1921 - 1942
  作者：Ruechardt,C.、Eichler,S.

  DOI：——

  日期：——