4,4-Dimethyl-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid | 1490229-33-8

• 分子结构分类: 有机化合物 - 脂质和类脂质分子 - 脂肪酰基
• 英文名称: 4,4-Dimethyl-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid
• CAS: 1490229-33-8
• 化学式: C₁₃H₂₅NO₄
• 分子量: 259.346
• InChiKey: CFYIQKCUPPEZNX-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  2.3
• 重原子数：
  18
• 可旋转键数：
  8
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.85
• 拓扑面积：
  75.6
• 氢给体数：
  2
• 氢受体数：
  4

反应信息

• 作为反应物：
  描述：

  4,4-Dimethyl-6-[(2-methylpropan-2-yl)oxycarbonylamino]hexanoic acid 、 3-溴丙烯 在 sodium hydride 作用下， 以 四氢呋喃 、 mineral oil 为溶剂， 反应 25.0h， 以68%的产率得到6-(allyl(tert-butoxycarbonyl)amino)-4,4-dimethylhexanoic acid
  参考文献：
  名称：

  Thermally induced substrate release via intramolecular cyclizations of Amino esters and Amino carbonates

  摘要：

  The relative cleavage of an alcohol from a panel of amino esters and amino carbonates via intramolecular cyclization was examined as a mechanism for substrate release. Thermal stability at 37 degrees C was observed only for the seven-membered ring progenitors. Applicability of the approach was illustrated by delta-lactam formation within a poly(dimethylsiloxane) microchannel for release of a captured fluorescent probe. (C) 2014 Elsevier Ltd. All rights reserved.

  DOI：

  10.1016/j.tet.2014.03.092

文献信息

• Thermally induced substrate release via intramolecular cyclizations of Amino esters and Amino carbonates
  作者：Ralph J. Knipp、Rosendo Estrada、Palaniappan Sethu、Michael H. Nantz

  DOI：10.1016/j.tet.2014.03.092

  日期：2014.5

  The relative cleavage of an alcohol from a panel of amino esters and amino carbonates via intramolecular cyclization was examined as a mechanism for substrate release. Thermal stability at 37 degrees C was observed only for the seven-membered ring progenitors. Applicability of the approach was illustrated by delta-lactam formation within a poly(dimethylsiloxane) microchannel for release of a captured fluorescent probe. (C) 2014 Elsevier Ltd. All rights reserved.