2-Ethyl-hexan-carbonsaeure-1-chlorid | 114182-65-9

• 分子结构分类: 有机化合物 - 有机卤素化合物 - 酰卤
• 英文名称: 2-Ethyl-hexan-carbonsaeure-1-chlorid
• 英文别名: 3-Ethylheptanoyl chloride
• CAS: 114182-65-9；114182-66-0；112604-84-9
• 化学式: C₉H₁₇ClO
• 分子量: 176.686
• InChiKey: URSDVOSFYLYSPT-UHFFFAOYSA-N

物化性质

• 沸点：
  204.6±8.0 °C(Predicted)
• 密度：
  0.950±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：
  6
• 环数：
  0.0
• sp3杂化的碳原子比例：
  0.89
• 拓扑面积：
  17.1
• 氢给体数：
  0
• 氢受体数：
  1

反应信息

• 作为反应物：
  描述：

  2-Ethyl-hexan-carbonsaeure-1-chlorid 在 氨 作用下， 生成 3-ethyl-heptanoic acid amide
  参考文献：
  名称：

  Graf,R., Justus Liebigs Annalen der Chemie, 1963, vol. 661, p. 111 - 157

  摘要：

  DOI：
• 作为产物：
  描述：

  3-乙基庚酸 在 氯化亚砜 作用下， 生成 2-Ethyl-hexan-carbonsaeure-1-chlorid
  参考文献：
  名称：

  Graf,R., Justus Liebigs Annalen der Chemie, 1963, vol. 661, p. 111 - 157

  摘要：

  DOI：

文献信息

• IMIDAZOPYRIMIDINES AND USES THEREOF
  申请人：Deadman John Joseph

  公开号：US20110028487A1

  公开（公告）日：2011-02-03

  The present invention provides a compound of formula (I) or a pharmaceutically acceptable derivative, salt or prodrug thereof. The present invention further provides a method of treatment or prophylaxis of a viral infection in a subject comprising administering to said subject an effective amount of a compound of formula (I) or a pharmaceutically acceptable derivative, salt or prodrug thereof. Pharmaceutical compositions comprising a compound of formula (I) are also provided.

  本发明提供了式（I）化合物或其药学上可接受的衍生物、盐或前药。本发明还提供了一种治疗或预防受体内病毒感染的方法，包括向该受体内注射有效量的式（I）化合物或其药学上可接受的衍生物、盐或前药。还提供了包括式（I）化合物的制药组合物。
• Fieser et al., Journal of the American Chemical Society, 1948, vol. 70, p. 3177
  作者：Fieser et al.

  DOI：——

  日期：——
• Improved Synthesis of Thienothiazole and Its Utility in Developing Polymers for Photovoltaics
  作者：Rycel Uy、Liqiang Yang、Huaxing Zhou、Samuel C. Price、Wei You

  DOI：10.1021/ma201835h

  日期：2011.12.13

  In response to the structural and electronic limitations of the popular benzo[1,2-b:4,5-b']dithiophene-thieno[3,4-b]thiophene (PBnDT-TT) polymer series, this study explores the design and synthesis of a thienothiazole (TTz) moiety. The synthesis of TTz was streamlined down to four high-yielding steps, resulting in the new polymer PBnDT-TTz for organic solar cells. By incorporating TTz, a nitrogen is directly introduced into the polymer backbone which tunes the HOMO level and eliminates the reliance on external substituents. Compared to its TT analogue, PBnDT-TTz exhibits the same HOMO level of -5.06 eV and the same V-oc of 0.69 eV, yet a higher power conversion efficiency of 2.5%. These promising results demonstrate the benefits of backbone modification and the great potential of TTz in the design of new polymers for organic photovoltaics.
• 3-Amino-1,2,4-triazolium salts as NHC-proligands: synthesis and postmodification of a new type of amino-functionalized Pd/NHC complexes
  作者：Dmitry V. Pasyukov、Andrey Yu. Chernenko、Konstantin E. Shepelenko、Vadim V. Kutyrev、Victor N. Khrustalev、Victor M. Chernyshev

  DOI：10.1016/j.mencom.2021.03.010

  日期：2021.3
• US3946054A
  申请人：——

  公开号：US3946054A

  公开（公告）日：1976-03-23