Acenaphthylene-1-carboxylic acid | 39653-73-1

• 分子结构分类: 有机化合物 - 苯类化合物 - 吖萘类
• 英文名称: Acenaphthylene-1-carboxylic acid
• 英文别名: Acenaphthylen-1-carbonsaeure；Acenaphthen-1-carbonsaeure
• CAS: 39653-73-1
• 化学式: C₁₃H₈O₂
• 分子量: 196.205
• InChiKey: GWVVKIJYUUCIDQ-UHFFFAOYSA-N

物化性质

• 沸点：
  357.1±11.0 °C(Predicted)
• 密度：
  1.417±0.06 g/cm3(Predicted)

计算性质

• 辛醇/水分配系数(LogP)：
  2.9
• 重原子数：
  15
• 可旋转键数：
  1
• 环数：
  3.0
• sp3杂化的碳原子比例：
  0.0
• 拓扑面积：
  37.3
• 氢给体数：
  1
• 氢受体数：
  2

反应信息

• 作为反应物：
  描述：

  Acenaphthylene-1-carboxylic acid 在 palladium on activated charcoal 氢气 作用下， 以 乙醇 为溶剂， 反应 3.0h， 以92%的产率得到1,2-二氢-1-苊羧酸
  参考文献：
  名称：

  An Efficient Synthesis of 1-Substituted Acenaphthylenes and Acenaphthenes, Synthesis of Acenaphthene-1-carboxylic acid

  摘要：

  DOI：

  10.1021/jo00099a047
• 作为产物：
  描述：

  Acenaphthylene ketone 在 水 作用下， 生成 Acenaphthylene-1-carboxylic acid
  参考文献：
  名称：

  Acenaphthyne

  摘要：

  DOI：

  10.1021/ja00413a074

文献信息

• Thia-tetraazaacenaphthylene kinase inhibitors
  申请人：Battista A. Kathleen

  公开号：US20070265264A1

  公开（公告）日：2007-11-15

  The present invention is directed to novel thia-tetraazaacenaphthylene compounds of Formula (I): and pharmaceutically acceptable forms thereof and their synthesis and use as inhibitors of ATP-protein kinase interactions.

  本发明涉及公式(I)的新型硫代四氮杂蒽化合物及其药学上可接受的形式，以及它们的合成和用作ATP-蛋白激酶相互作用抑制剂的用途。
• Anti-reflection coating forming composition
  申请人：——

  公开号：US20020086934A1

  公开（公告）日：2002-07-04

  An anti-reflection coating-forming composition is provided. This composition includes a polymer and a solvent. The polymer has a structural unit represented by the formula (1): 1 wherein R 1 is a monovalent atom other than a hydrogen atom or a monovalent group, and n is an integer of 0-4, provided that when n is an integer of 2-4, a plural number of R 1 's are the same or different; R 2 and R 3 are each a monovalent atom or group; and X is a bivalent group. The anti-reflection coating formed from this composition has a high antireflective effect, does not generate intermixing with a resist film, and enables a good resist pattern profile excellent in resolution and precision in cooperation with a positive or negative resist.

  提供了一种抗反射涂层形成组合物。这种组合物包括一种聚合物和一种溶剂。聚合物具有由式（1）表示的结构单元： 1 其中 R 1 是氢原子或一价基团以外的一价原子，n 是 0-4 的整数，但当 n 是 2-4 的整数时，R 1 的复数相同或不同；R 2 和 R 3 均为一价原子或基团；X 为二价基团。由这种组合物形成的抗反射涂层具有很高的抗反射效果，不会与抗蚀剂薄膜产生混杂，并且在与正极或负极抗蚀剂配合使用时，可以形成分辨率和精度极佳的抗蚀图案轮廓。
• Structural requirements for substrate in highly enantioselective hydrogenation over the cinchonidine-modified Pd/C
  作者：Takashi Sugimura、Takayuki Uchida、Junya Watanabe、Takeshi Kubota、Yasuaki Okamoto、Tomonori Misaki、Tadashi Okuyama

  DOI：10.1016/j.jcat.2008.11.022

  日期：2009.2.15

  Relationship between substrate Structure and enantioselectivity is studied for the asymmetric hydrogenation of 42 different (E)-alpha, beta-disubstituted acrylic acids (propenoic acids) over cinchonidine-modified Pd/C. The beta-phenyl group is indispensable for high enantioselectivity of alpha-phenylcinnamic acid (2,3-diphenylpropenoic acid, 81% ee), and substitution on this group affects markedly the selectivity. The high ee up to 92% was achieved by the beta-p-alkoxyphenyl substitution, and the selectivity is ascribed mainly to stronger interaction of the substrate with the chiral modifier on the catalyst surface. In contrast, substitution on the alpha-phenyl group does not affect notably the enantioselectivity (80-82% ee) or even the alpha-phenyl group itself is not indispensable but replaceable with a properly bulky group for the high enantioselectivity, (C) 2008 Elsevier Inc. All rights reserved.
• Konstitution und konfiguration der photodimeren 1-substituierter acenaphthylene
  作者：H Mayer、J Sauer

  DOI：10.1016/s0040-4039(00)88270-2

  日期：1983.1
• Haddad Nizar, Abu-Shqara Elias, J. Org. Chem., 59 (1994) N 20, S 6090-6092
  作者：Haddad Nizar, Abu-Shqara Elias

  DOI：——

  日期：——