2,6-dipropionyl-pyridine | 36763-34-5

• 分子结构分类: 有机化合物 - 有机氧化合物
• 英文名称: 2,6-dipropionyl-pyridine
• 英文别名: 2,6-Dipropionyl-pyridin；1,1'-(Pyridine-2,6-diyl)bis(propan-1-one)；1-(6-propanoylpyridin-2-yl)propan-1-one
• CAS: 36763-34-5
• 化学式: C₁₁H₁₃NO₂
• 分子量: 191.23
• InChiKey: QRNBZSPPOLUSJO-UHFFFAOYSA-N

计算性质

• 辛醇/水分配系数(LogP)：
  1.8
• 重原子数：
  14
• 可旋转键数：
  4
• 环数：
  1.0
• sp3杂化的碳原子比例：
  0.36
• 拓扑面积：
  47
• 氢给体数：
  0
• 氢受体数：
  3

反应信息

• 作为反应物：
  描述：

  2,6-dipropionyl-pyridine 在 一水合肼 作用下， 生成 2,6-二丙基吡啶
  参考文献：
  名称：

  Lukes; Pergal, Collection of Czechoslovak Chemical Communications, 1959, vol. 24, p. 36,43

  摘要：

  DOI：
• 作为产物：
  描述：

  吡啶-2,6-二甲酰胺 在 乙醚 、 三氯氧磷 作用下， 生成 2,6-dipropionyl-pyridine
  参考文献：
  名称：

  Lukes; Pergal, Collection of Czechoslovak Chemical Communications, 1959, vol. 24, p. 36,43

  摘要：

  DOI：

文献信息

• A Self-Associating ADADA Hydrogen-Bonded Double Helix
  作者：Jiaxin Li、James A. Wisner、Michael C. Jennings

  DOI：10.1021/ol071171c

  日期：2007.8.1

  We report the design, synthesis, and characterization of an oligomer which incorporates a non-coplanar ADADA (hydrogen bond donor/acceptor) array within its structure. The molecule associates through self-complementary hydrogen bonding to form a dimeric double-helical complex.
• Bachmann; Jenkins, Journal of the American Pharmaceutical Association (1912), 1951, vol. 40, p. 44
  作者：Bachmann、Jenkins

  DOI：——

  日期：——
• Preparation of supramolecular polymers containing sequence-selective hydrogen bonding subunits in their backbone which form double helices
  申请人：Wisner James Andrew

  公开号：US20090318626A1

  公开（公告）日：2009-12-24

  The present invention relates to supramolecular polymers containing sequence-selective hydrogen bonding subunits in their backbone which form double helices. The invention allows for tuning of the numbers and sequences of donor/acceptor units incorporated in any one crosslinking hydrogen bonding subunit and hence tuning of the interaction strength not only through the amount of crosslinking material incorporated but also through modulation of the strength of the crosslinking interactions. It also allows for the incorporation of more than one type of crosslinking agent in the material allowing for multiple strengths of crosslinking which are each tunable with regard to disruption from solvent, temperature and stress. Hydrogen bond strength between oligomeric chains can be tailored through modification of the numbers and sequences of the donors/acceptors in the oligomers. The oligomers are sequence-specific and will generally only hydrogen-bond to oligomeric chains which are composed of a complementary set of donors/acceptors. The hydrogen bonded motif formed by the interacting oligomers is helical, imparting both chirality and intertwined topology to these interaction points. Because the polymer end units react with their complements through hydrogen bonding, the telechelic polymer(s) incorporating this technology are reversibly able to be processed as the bonds are first broken and then reformed. This has applications in a number of fields such as inkjet inks, adhesives, printing plates and microphase patterning of polymer surfaces.
• Anti-Heparin Compounds
  申请人：Scott Richard W.

  公开号：US20110178104A1

  公开（公告）日：2011-07-21

  The present invention provides compounds and methods for antagonizing the anticoagulant effect of an anticoagulant agent that is selected from UFH, LMWH, and a heparin/LMWH derivative in a patient comprising administering to the patient a compound of the invention or a salt thereof, or a composition comprising the same.
• ORGANIC ELECTROLUMINESCENT DEVICE
  申请人：Kuramochi Yusuke

  公开号：US20120049167A1

  公开（公告）日：2012-03-01

  An organic electroluminescent device in which an organic layer containing a metal coordination compound represented by the following formula (1) is sandwiched between the pair of electrodes composed of an anode and a cathode, ML a X b (1) wherein M is an ion of a metal of Group 11 of the Periodic Table, L is a ligand represented by the formula (2) shown below, X is an anion, and a and b are defined in the specification, wherein A is a divalent group formed by removing two hydrogen atoms from the formula (3) or (4) shown below, and D 1 , k 1 , m 1 , A, D 1 , Q 1 , and Q 2 are defined in the specification, wherein X 1 , X 2 , X 3 , X 4 , X 5 , R 1 , R 5 , R 6 , and R 9 are defined in the specification.

表征谱图