2-[2,4-二(叔丁基)苯氧基]-5,5-二甲基-1,3,2-二氧杂磷杂环己烷 | 71519-95-4

• 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-[2,4-二(叔丁基)苯氧基]-5,5-二甲基-1,3,2-二氧杂磷杂环己烷
• 中文别名: 3-[2-(十二烷氧基)乙氧基]丙腈
• 英文名称: 2-(2,4-di-tert-butyl-phenoxy)-5,5-dimethyl-1,3,2-dioxaphosphrinane
• 英文别名: 2-(2,4-bis(tert-butyl)phenoxy)-5,5-dimethyl-1,3,2-dioxaphosphorinane；1,3,2-Dioxaphosphorinane, 2-[2,4-bis(1,1-dimethylethyl)phenoxy]-5,5-dimethyl-；2-(2,4-ditert-butylphenoxy)-5,5-dimethyl-1,3,2-dioxaphosphinane
• CAS: 71519-95-4
• 化学式: C₁₉H₃₁O₃P
• 分子量: 338.427
• InChiKey: DLOCWLUOVMSSII-UHFFFAOYSA-N

物化性质

• 沸点：
  346.1±42.0 °C(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  6.2
• 重原子数：
  23
• 可旋转键数：
  4
• 环数：
  2.0
• sp3杂化的碳原子比例：
  0.68
• 拓扑面积：
  27.7
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2-[2,4-二(叔丁基)苯氧基]-5,5-二甲基-1,3,2-二氧杂磷杂环己烷 生成 2-(2,4-ditert-butylphenoxy)-5,5-dimethyl-1,3,2λ5-dioxaphosphinane 2-oxide
  参考文献：
  名称：

  KONIG, T.;HABICHER, W. D.;SCHWETLICK, K., J. PRAKT. CHEM., 331,(1989) N, C. 913-922

  摘要：

  DOI：

文献信息

• KONIG, T.;HABICHER, W. D.;SCHWETLICK, K., J. PRAKT. CHEM., 331,(1989) N, C. 913-922
  作者：KONIG, T.、HABICHER, W. D.、SCHWETLICK, K.

  DOI：——

  日期：——
• Process For Preparing A Polypropylene-Based Object Having An Increased Surface Energy
  申请人：CLARIANT INTERNATIONAL LTD

  公开号：US20150252066A1

  公开（公告）日：2015-09-10

  Process for preparing a polypropylene-based object having an increased surface energy The present invention relates to a process for preparing a polypropylene-based object having an increased surface energy, said process comprising the subsequent steps of a) providing a polypropylene resin, b) forming an object of said polypropylene resin, and c) subjecting the surface of the object to a surface energy increasing treatment step, Characterized in that the polypropylene resin comprises A) at least one secondary antioxidant of formula (I) in which n is 0 or 1, each R may be the same or different and is an unsubstituted phenyl group or a phenyl group substituted by one or two alkyl groups having from 1 to 12 carbon atoms, and X is a residue of a monofunctional or difunctional phenyl group, diphenyl group, diphenyl ether group or dibenzofuranyl group and/or of formula (II)